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Device Explorer · FDA GUDID · GMDN 35380

Tendon stripper

A hand-held manual surgical instrument designed to excise a length of ligament, tendon or fascia for use as a living graft. It typically consists of a handle and a semicircular shaped trough that terminates in a sharp cutting edge. It is typically made of high

US‑registered devices383in commercial distribution
Companies42labelers on GUDID
Single‑use6%of device records
Sterile4%labelled sterile
Prescription66%Rx‑only share
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Share of device records

Avalign Technologies, Inc.5815%
Ambler Surgical Corp.369%
Buxton Biomedical, Inc.246%
Arthrex, Inc.226%
Accurate Surgical & Scientific Instruments Corporation195%
Surtex Instruments Ltd.174%
Boss Instruments, Ltd., Inc.174%
Surgical Direct, Inc.174%

Top labelers

CompanyDevicesShare
Avalign Technologies, Inc.5815%
Ambler Surgical Corp.369%
Buxton Biomedical, Inc.246%
Arthrex, Inc.226%
Accurate Surgical & Scientific Instruments Corporation195%
Surtex Instruments Ltd.174%
Boss Instruments, Ltd., Inc.174%
Surgical Direct, Inc.174%
Integra Lifesciences Production Corporation174%
Sklar Corporation144%
Biomet Microfixation, Inc123%
Rz-Medizintechnik Gmbh113%

Company = labeler of record on GUDID. 42 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

VersiQuadRELIANCESurtexNAN/ARZ Medizintechnik GmbHn.a.MediconLIGAFIXArthrex®BOSS InstrumentsSTRIPPEROpen EndedTendon StripperSymmetry BunnellSymmetry Brand

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
HRTSTRIPPER, SURGICAL177
HRTStripper, Surgical75
MDMInstrument, Manual, Surgical, General Use30
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT21
GAISTRIPPER, VEIN, REUSABLE14
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE12

GMDN & GCC registration

  • GMDN code 35380 · non‑implantable
  • Single‑use 6% · sterile 4% · Rx‑only 66% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 18Length (Centimeter) · 5Length (Millimeter) · 2

Use these as the dimensions to specify in a tender line.

How many tendon stripper products are registered in the US?

383 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Tendon stripper", from 42 companies. The largest labeler is Avalign Technologies, Inc. with 15% of records.

Which FDA product codes apply?

HRT (STRIPPER, SURGICAL), HRT (Stripper, Surgical), MDM (Instrument, Manual, Surgical, General Use), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT)

Is this the same as UAE/GCC registration?

No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.

How do I get quotes?

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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.

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