Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › ENT soft-tissue cutting forceps
Device Explorer · FDA GUDID · GMDN 36199

ENT soft-tissue cutting forceps

A hand-held manual surgical instrument with a biting action intended to be used to punch/cut/excise soft-tissue during an ear/nose/throat (ENT) procedure [e.g., adenoidectomy, tonsillectomy, sinus surgery, septoplasty, and/or biopsy]. It is a metallic instrume

US‑registered devices1,391in commercial distribution
Companies35labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription70%Rx‑only share
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Share of device records

Princeton Medical Group, Inc.26819%
Br Surgical, Llc14010%
Boss Instruments, Ltd., Inc.13310%
Ambler Surgical Corp.1319%
Fentex Medical Gmbh1148%
Integra Lifesciences Production Corporation876%
Med Saver, Inc.866%
Karl Storz Gmbh & Co. Kg765%

Top labelers

CompanyDevicesShare
Princeton Medical Group, Inc.26819%
Br Surgical, Llc14010%
Boss Instruments, Ltd., Inc.13310%
Ambler Surgical Corp.1319%
Fentex Medical Gmbh1148%
Integra Lifesciences Production Corporation876%
Med Saver, Inc.866%
Karl Storz Gmbh & Co. Kg765%
Avalign Technologies, Inc.705%
Rz-Medizintechnik Gmbh423%
Bausch & Lomb Incorporated332%
Sontec Instruments, Inc.272%

Company = labeler of record on GUDID. 35 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Collin tongue forcepsBraun hook forcepsWhite tonsil forcepsColver tonsil forcepsBlohmke tonsil forcepsMikulicz tonsil forcepsOverholt-Geissdoerfer tonsil forcepsNegus tonsil forcepsSchnidt tonsil forcepsFENTEXForeign body forcepsRZ Medizintechnik GmbHRHINOFORCEn.a.SilCutAESCULAP

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

FDA product codes

CodeNameDevices
KAEFORCEPS, ENT303
HTDForceps268
LRCINSTRUMENT, ENT MANUAL SURGICAL261
KAEForceps, Ent135
KAWPUNCH, ANTRUM122
KTFPUNCH, ENT105

GMDN & GCC registration

  • GMDN code 36199 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 70% · 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) · 42Width (Millimeter) · 33Angle (degree) · 19Outer Diameter (Millimeter) · 12Length (Millimeter) · 8Length (Centimeter) · 7

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

How many ent soft-tissue cutting forceps products are registered in the US?

1,391 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "ENT soft-tissue cutting forceps", from 35 companies. The largest labeler is Princeton Medical Group, Inc. with 19% of records.

Which FDA product codes apply?

KAE (FORCEPS, ENT), HTD (Forceps), LRC (INSTRUMENT, ENT MANUAL SURGICAL), KAE (Forceps, Ent)

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.

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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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