Consulting Wallah › Device Explorer › Catheters & tubes › Airway tube forceps, reusable
Device Explorer · FDA GUDID · GMDN 31264

Airway tube forceps, reusable

A hand-held instrument used for grasping a tube [e.g., a catheter or an endotracheal (ET) tube] for its insertion and/or extraction into/from the airways, or for grasping obstructive objects for their removal from the airways. Commonly known as a Magill's forc

US‑registered devices95in commercial distribution
Companies21labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription51%Rx‑only share
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Share of device records

Sklar Corporation2728%
Boss Instruments, Ltd., Inc.77%
Anesthesia Associates, Inc.77%
Br Surgical, Llc66%
Ambler Surgical Corp.66%
Integra Lifesciences Production Corporation66%
Medicon Eg. Chirurgiemechaniker-Genossenschaft55%
Professional Surgical Instruments Co., Inc.55%

Top labelers

CompanyDevicesShare
Sklar Corporation2728%
Boss Instruments, Ltd., Inc.77%
Anesthesia Associates, Inc.77%
Br Surgical, Llc66%
Ambler Surgical Corp.66%
Integra Lifesciences Production Corporation66%
Medicon Eg. Chirurgiemechaniker-Genossenschaft55%
Professional Surgical Instruments Co., Inc.55%
Fentex Medical Gmbh33%
Kls-Martin L.P.33%
Gsource Llc33%
Sontec Instruments, Inc.33%

Company = labeler of record on GUDID. 21 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FENTEXRZ Medizintechnik GmbHMediconBOSS InstrumentsFORCEPSProfessional Surgical Instruments Co., Inc.ASSIgSourceBR Surgical, LLCMcKessonMSI Precision Specialty InstrumentsCHEST TUBE PASSERMillenniumAvalignAmbler Value LineAmbler Surgical

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

FDA product codes

CodeNameDevices
GENFORCEPS, GENERAL & PLASTIC SURGERY35
BWBFORCEPS, TUBE INTRODUCTION22
BWBForceps, Tube Introduction11
HTDForceps9
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE7
HTDFORCEPS6

GMDN & GCC registration

  • GMDN code 31264 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 51% · 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) · 4Length (Centimeter) · 1

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

How many airway tube forceps, reusable products are registered in the US?

95 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Airway tube forceps, reusable", from 21 companies. The largest labeler is Sklar Corporation with 28% of records.

Which FDA product codes apply?

GEN (FORCEPS, GENERAL & PLASTIC SURGERY), BWB (FORCEPS, TUBE INTRODUCTION), BWB (Forceps, Tube Introduction), HTD (Forceps)

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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