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Device Explorer · FDA GUDID · GMDN 33433

ENT probe, reusable

A slender, rod-like, hand-held manual surgical instrument, typically with a blunt bulbous or pointed tip, used for exploring fistulas, cavities or wounds used during ear/nose/throat (ENT) intervention. The distal end of the instrument, before the bulb/point, m

US‑registered devices187in commercial distribution
Companies12labelers on GUDID
Single‑use18%of device records
Sterile2%labelled sterile
Prescription53%Rx‑only share
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Share of device records

Gsource Llc3418%
Sklar Corporation3217%
Medicon Eg. Chirurgiemechaniker-Genossenschaft3016%
Seaspine Orthopedics Corporation2815%
Mizuho America, Inc.169%
Karl Storz Gmbh & Co. Kg126%
Jedmed Instrument Company116%
Spiggle & Theis Medizintechnik Gmbh84%

Top labelers

CompanyDevicesShare
Gsource Llc3418%
Sklar Corporation3217%
Medicon Eg. Chirurgiemechaniker-Genossenschaft3016%
Seaspine Orthopedics Corporation2815%
Mizuho America, Inc.169%
Karl Storz Gmbh & Co. Kg126%
Jedmed Instrument Company116%
Spiggle & Theis Medizintechnik Gmbh84%
Ambler Surgical Corp.84%
Aztecmed/Ent Llc42%
Teleflex Incorporated32%
Avalign Technologies, Inc.11%

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

Brand names on the register (sample)

Salivary duct probeBall-end probeKocher directorHollow probeBowman salivary duct probeSalivary duct probe set, double endedProbe, bluntNasal proben.a.MedicongSourceTeardrop Probe, 45 Degrees Down, Bayonet, 11cm WTeardrop Probe, 90 Degrees Up, Bayonet, 11cm WLTeardrop Probe, 45 Degrees Up, Bayonet, 11cm WLTeardrop Probe, Straight, Bayonet, 11cm WLTeardrop Probe, 45 Degrees Down, Bayonet, 9cm WL

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

FDA product codes

CodeNameDevices
HXBPROBE70
MDMInstrument, Manual, Surgical, General Use41
KAKPROBE, ENT24
LRCINSTRUMENT, ENT MANUAL SURGICAL13
HXBProbe9
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE8

GMDN & GCC registration

  • GMDN code 33433 · non‑implantable
  • Single‑use 18% · sterile 2% · Rx‑only 53% · 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) · 3

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

How many ent probe, reusable products are registered in the US?

187 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "ENT probe, reusable", from 12 companies. The largest labeler is Gsource Llc with 18% of records.

Which FDA product codes apply?

HXB (PROBE), MDM (Instrument, Manual, Surgical, General Use), KAK (PROBE, ENT), LRC (INSTRUMENT, ENT MANUAL SURGICAL)

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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