Consulting Wallah › Device Explorer › Endoscopy & surgical instruments › ENT foreign body extraction forceps
Device Explorer · FDA GUDID · GMDN 65449

ENT foreign body extraction forceps

A hand-held, manual, non-surgical device intended to be inserted into the nasal or ear canal to grip and extract a foreign body/debris (e.g., ear wax) during an ear/nose/throat (ENT) procedure; it is not intended for surgical grasping or manipulation of tissue

US‑registered devices61in commercial distribution
Companies11labelers on GUDID
Single‑use39%of device records
Sterile18%labelled sterile
Prescription74%Rx‑only share
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Share of device records

Bausch & Lomb Incorporated1423%
Fentex Medical Gmbh1220%
Jedmed Instrument Company915%
Dtr Medical Limited610%
Eakin Surgical Limited58%
Sunmed, Llc58%
Adept Medical Limited47%
Bionix, Llc35%

Top labelers

CompanyDevicesShare
Bausch & Lomb Incorporated1423%
Fentex Medical Gmbh1220%
Jedmed Instrument Company915%
Dtr Medical Limited610%
Eakin Surgical Limited58%
Sunmed, Llc58%
Adept Medical Limited47%
Bionix, Llc35%
Marina Medical Instruments, Inc.12%
Br Surgical, Llc12%
Ear Technology Corporation12%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Crocodile Forceps, 6.75mm jaw, steel finishOrmerod Forceps, black finishHenckel Aural ForcepsCrocodile Fine Jaw Micro Forceps, black finishCrocodile Micro Forceps, black finishCrocodile Micro Forceps, steel finishSingle Use ProfessionalFENTEXReplacement Forceps without Light SourceLighted Forceps for Foreign Body RemovalMarina MedicalBR Surgical, LLCLightBeamBausch + LombSample, Lighted Forceps for Foreign Body RemovalSunMed

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

FDA product codes

CodeNameDevices
KAEForceps, Ent30
LRCINSTRUMENT, ENT MANUAL SURGICAL12
KAEFORCEPS, ENT8
GENFORCEPS, GENERAL & PLASTIC SURGERY4
GENForceps, General & Plastic Surgery4
HTDFORCEPS1

GMDN & GCC registration

  • GMDN code 65449 · non‑implantable
  • Single‑use 39% · sterile 18% · Rx‑only 74% · 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 (Millimeter) · 1Length (Inch) · 1

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

How many ent foreign body extraction forceps products are registered in the US?

61 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "ENT foreign body extraction forceps", from 11 companies. The largest labeler is Bausch & Lomb Incorporated with 23% of records.

Which FDA product codes apply?

KAE (Forceps, Ent), LRC (INSTRUMENT, ENT MANUAL SURGICAL), KAE (FORCEPS, ENT), GEN (FORCEPS, GENERAL & PLASTIC SURGERY)

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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