Supplier Qualification & Company Profile

Supplier Qualification & Company Profile

EndoTech Group of Industries manufactures surgical instruments in Sialkot, Pakistan. This supplier profile gives importers, distributors, healthcare supply companies and purchasing teams a practical overview of our company identity, product categories, manufacturing capabilities and the documentation to request during supplier qualification.

Use this page to assess basic supplier fit and prepare a document request before moving into product-specific quotation and technical review.

Established 1990 Sialkot, Pakistan International B2B Supply Surgical & Dental Instruments
EndoTech surgical instrument manufacturing facility in Sialkot Pakistan
Supplier Profile Company information, product coverage, supplier documentation and procurement contact details in one place.
1990 Manufacturing history beginning in 1990
55 Countries reported as served
350 Employees reported on the company website
70 Clients reported on the company website
10,000 Instrument types reported on the company website

These figures are published in EndoTech's public company profile. Confirm the current workforce, client count, export reach and instrument-range total internally before using them in formal vendor onboarding or procurement submissions. They are not monthly production-output figures.

Manufacturer Identity

Company Information for Supplier Onboarding

Start with the manufacturer's identity, location and scope. For formal onboarding, confirm the details against the current company registration documents and the exact legal entity named in the purchasing agreement.

Company & Manufacturer Details

  • Public company identity EndoTech Group of Industries
  • Manufacturer name shown in supplied certificate records ENDO TECH INSTRUMENTS
  • Operating location Sialkot, Punjab, Pakistan
  • Factory / business address Al-Muslim Street #5, Islam Nagar Road, Pacca Garah, Sialkot – 51310, Pakistan
  • Manufacturing history Company website states manufacturing began in 1990.
The public brand name and the manufacturer name printed on certificate records are shown separately for clarity. Formal buyers should confirm the current registered legal entity, registration number and tax details directly from the relevant company documents.

What a Purchasing Team Should Confirm

Before approving a new supplier, make sure the records supplied by the manufacturer match the entity that will manufacture, invoice and supply the products.

  • Legal identity Current legal company name and applicable registration evidence.
  • Physical location Factory and correspondence details relevant to the transaction.
  • Product scope Instrument categories and SKUs relevant to the planned order.
  • Quality documents Current documents with scope matching the entity and activities.
  • Commercial contact A responsible contact for quotes, documentation and order communication.
EndoTech company profile and surgical instrument quality information
Company Background

An Established Surgical Instrument Manufacturer in Sialkot

EndoTech's published company history states that precision surgical instrument manufacturing began in 1990 as a family business and has continued into a second generation.

The company describes its customers as including hospitals, distributors and healthcare brands in international markets, with established wholesale and medical supply relationships in the United States.

For procurement teams, the next step is to match this background information with current company records, product requirements and the quality documentation needed for the intended market.

  • Surgical instrument manufacturing and export
  • Multiple product categories under one supplier
  • OEM and private-label manufacturing services
  • Quality review described across production stages

Read the full company background →

Product Portfolio

Surgical & Dental Instrument Categories

EndoTech's current website organizes its products into the following main categories. Buyers should confirm the exact product models, specifications and manufacturing availability during technical review.

ENT Instruments

ENT instruments including forceps, nasal specula, ear curettes, punches and related instruments.

Explore ENT instruments →

Surgical Retractors

Retractor families including Weitlaner, Mollison, Beckmann, Gelpi and Collin.

Explore retractor instruments →

Orthopedic Instruments

Product categories include bone surgery, bone holding forceps, bone rongeurs, surgical mallets, extraction pliers, wire cutting pliers and osteotomes.

Explore orthopedic instruments →

Gynecology Instruments

The published category includes biopsy forceps, Tischler biopsy forceps and cervical biopsy instruments.

Explore gynecology instruments →

Kerrison Rongeur

The current catalogue structure includes Kerrison punch and disc rongeur product categories.

Explore Kerrison instruments →

Dental Instruments

Dental product areas include implantology, anaesthesia, orthodontics, extraction, impression, diagnostics, restorative dentistry, surgery and periodontal instruments.

Explore dental instruments →
Surgical instrument quality inspection at EndoTech
Manufacturing & Quality

Understand the Production Capability Behind Your Order

EndoTech's published manufacturing information describes a production flow that includes material selection, forging, machining, hand-making, setting, finishing, measurement and final inspection. The exact sequence varies by instrument.

For supplier qualification, buyers should confirm which processes are used for their particular product, which operations are performed in-house and which, if any, are handled by external suppliers.

Production Forging, forming and machining as applicable.
Workmanship Skilled hand operations and finishing where required.
Measurement Defined product dimensions and critical features.
Final Review Inspection against applicable requirements.

Review manufacturing strength and process →

Review quality assurance and inspection →

Supplier Evidence

Review Evidence Before Approving a Supplier

Use current, relevant documentation to assess the supplier. A company profile or a certificate image is a starting point, not a substitute for verifying the exact legal entity, document scope, validity and product requirements.

Quality & Certification Documents

Request the current quality-system certificates and applicable regulatory documents relevant to the legal manufacturer, product category and destination market.

Review certification information →

Inspection & Quality Process

Review the quality inspection stages and confirm which product-specific checks, records and reports are maintained and available for the order being evaluated.

Review quality assurance →

U.S. Importer Documentation

U.S. buyers should verify the current establishment, device-specific regulatory pathway, labeling and import documentation applicable to the exact device.

Review U.S. documentation guidance →
Certificate validity: The certificate images previously supplied for EndoTech's website show historical validity periods ending in December 2024. Request the current certificate set before relying on any certificate for vendor approval, regulatory review or procurement in 2026.
Supplier Qualification Pack

Documents to Request During Vendor Onboarding

Purchasing teams can use the checklist below to prepare a supplier approval file. Availability, current validity and relevance should be confirmed with EndoTech for each request.

01. Company Identity

Use these records to confirm which entity you are qualifying and which company will enter the purchase agreement.

  • Current legal company name and applicable registration evidence
  • Registered or business address
  • Applicable tax or business registration details
  • Authorized commercial contact details
  • Current company profile or supplier questionnaire

02. Quality & Regulatory Documents

Confirm which current records are relevant to the products and destination market.

  • Current quality-management certificates, where applicable
  • Applicable product declarations and regulatory records
  • Relevant FDA establishment and device listing details, where applicable
  • Product-specific regulatory pathway information
  • Applicable labeling and technical documents

03. Manufacturing & Quality Capability

Establish whether the supplier can manufacture and inspect the product to your required specification.

  • Product catalogue and relevant SKUs
  • Material and product specifications
  • Manufacturing and inspection process details
  • Applicable inspection records or sample reports
  • Subcontracting and process-control information, where relevant

04. Commercial & Delivery Information

Confirm whether the operating and commercial arrangements meet your purchasing requirements.

  • MOQ by product or product family
  • Sampling requirements and charges, where applicable
  • Current estimated lead times for the order
  • Packaging and shipment arrangements
  • Payment terms and order conditions
Document confidentiality: Share confidential records through an agreed business channel. Do not publish customer agreements, banking details, private customer contacts or unredacted inspection documents on the public website.
Procurement Workflow

A Practical Supplier Qualification Process

Use a defined process to move from an initial company review to a product-specific sourcing decision.

Step 01

Define Your Requirement

Identify the instrument category, expected product mix, intended market and estimated order volumes.

Step 02

Review Company Documents

Check the company identity, address, current quality documents and applicable regulatory information.

Step 03

Assess Product Capability

Review specifications, sampling requirements, quality criteria, capacity and delivery expectations.

Step 04

Approve the Supplier

Complete your internal review, resolve outstanding questions and document the approved scope of supply.

Production & Order Planning

Confirm Capacity Against Your Actual Product List

Supplier capacity should be assessed against the instruments, specifications and delivery requirements you actually intend to purchase, rather than through a single generic factory output number.

Product-Specific Capacity

Ask for estimated production quantities and lead times by product or SKU. Different instruments require different processes, work content, inspection and scheduling.

For larger sourcing programs, discuss whether the requested products can be produced concurrently or need to be scheduled in separate batches.

Repeat-Order Planning

For ongoing supply, confirm the product specification, repeat-order lead times, sample-approval process, packaging requirements and how changes to the order will be handled.

These details are more useful to procurement planning than an unverified claim about maximum monthly factory output.

Capacity disclosure: EndoTech's public homepage lists workforce and product-range figures, but it does not establish a verified monthly production output for each category. Request a current, product-specific capacity and lead-time statement when qualifying the supplier for a defined purchase program.
Supplier Enquiries

Contact EndoTech for Supplier Qualification

Send the product categories you are sourcing, the destination market and the documents required by your procurement team. EndoTech can then review the request and confirm what information is available.

Company Contact Information

Use the published company contact channels for supplier onboarding, product enquiries and documentation requests.

Business / Factory Address Al-Muslim Street #5, Islam Nagar Road,
Pacca Garah, Sialkot – 51310, Pakistan
General Enquiries info@endotech.com.pk
Customer Service ghafar@endotech.com.pk

What to Include in Your Enquiry

To help the team respond to a qualification request, include the basic information your purchasing team already has available.

  • Your company Company name, country and purchasing contact.
  • Products Category, catalogue reference or SKU list.
  • Market USA or other destination market.
  • Order plan Estimated quantities, sampling needs and target schedule.
  • Documents List the company, quality, product or regulatory documents you need.
Supplier Qualification FAQ

Frequently Asked Questions

Practical information for companies evaluating EndoTech as a surgical instrument supplier.

What is EndoTech's manufacturing history?
EndoTech's public company profile states that surgical instrument manufacturing began in 1990 in Sialkot, Pakistan.
What is the manufacturer's name?
The public company identity is EndoTech Group of Industries. The certificate records previously supplied for the website show the manufacturer name as ENDO TECH INSTRUMENTS. Formal purchasing and vendor records should use the exact current legal entity name confirmed by EndoTech's current company documents.
What surgical instrument categories does EndoTech offer?
The published website categories include ENT, surgical retractors, orthopedics, gynecology, Kerrison Rongeur and dental instruments. Buyers should confirm the exact SKUs, specifications and availability for their project.
What documents should I request to qualify EndoTech as a supplier?
Depending on your onboarding requirements, request company registration information, current quality certificates, product-specific regulatory documents, product specifications, relevant inspection records and commercial information such as MOQ and delivery estimates. Confirm each document's availability and applicable scope directly with EndoTech.
Can EndoTech provide a company profile PDF?
Contact EndoTech to request a current company profile PDF or supplier-information pack for your vendor onboarding. The public website provides company and catalogue information, but availability of a separate supplier-profile PDF should be confirmed by the company.
How many employees does EndoTech have?
The company's current public homepage lists 350 employees. Purchasing teams that need a verified workforce figure for a formal supplier audit or tender should request an updated company profile or supporting confirmation.
What is EndoTech's monthly production capacity?
The public company profile does not establish a verified monthly production figure for each category. Request a current capacity and lead-time estimate for your product list, specifications and order quantities.
Are the certificate images on the website sufficient for approval?
Not by themselves. Buyers should request current certificates, verify the issuing organization and scope, and confirm that the documents apply to the relevant manufacturer, activity and product. Historical certificate images should not be treated as evidence of present validity without further verification.
Can EndoTech be considered for U.S. importer or distributor supply?
EndoTech's published company profile describes international distribution relationships, including in the United States. U.S. buyers should still assess the relevant product documentation, current regulatory pathway, commercial terms and supplier qualifications for their intended transaction.
How do I start the supplier qualification process?
Send EndoTech your company details, destination market, product categories, estimated quantities and requested documents. The team can review the enquiry and clarify which supplier and product information is available.
Start Supplier Evaluation

Evaluating EndoTech for Your Next Surgical Instrument Program?

Send your product list, destination market and supplier qualification checklist. EndoTech can review the sourcing requirements and discuss the relevant company, product, quality and commercial information for your project.

EndoTech Group of Industries · Sialkot, Pakistan · Surgical & Dental Instrument Manufacturing