Consulting Wallah › Device Explorer › Other devices › Abdominal/ENT/orthopaedic surgical probe, reusable
Device Explorer · FDA GUDID · GMDN 47862

Abdominal/ENT/orthopaedic surgical probe, reusable

A slender, rod-like, hand-held manual surgical instrument intended to be used to explore cavities, wounds or fistulas during abdominal, ENT, and/or orthopaedic surgical interventions; it does not include stereotactic devices and is not dedicated to endoscopy.

US‑registered devices2,356in commercial distribution
Companies111labelers on GUDID
Single‑use5%of device records
Sterile0%labelled sterile
Prescription86%Rx‑only share
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Share of device records

Medtronic Sofamor Danek, Inc.27912%
Alphatec Spine, Inc.26411%
Depuy Spine, Llc2149%
Cg Medtech Co.,Ltd.904%
Flospine Llc874%
Integra Lifesciences Production Corporation844%
Highridge Medical, Llc813%
Seaspine Orthopedics Corporation773%

Top labelers

CompanyDevicesShare
Medtronic Sofamor Danek, Inc.27912%
Alphatec Spine, Inc.26411%
Depuy Spine, Llc2149%
Cg Medtech Co.,Ltd.904%
Flospine Llc874%
Integra Lifesciences Production Corporation844%
Highridge Medical, Llc813%
Seaspine Orthopedics Corporation773%
Aesculap Ag723%
Biomet Uk Ltd572%
Novo Surgical, Inc.512%
Avalign Technologies, Inc.502%

Company = labeler of record on GUDID. 111 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

OASYSRELIANCE LITeXIA 3XIAXIA 4.5CarboClear Posterior Cervical Screw SystemFeeler Gauge - ThickFeeler Gauge - ThinStraight Pedicle Probe XLPedicle Probe XLNon-Tapered Pedicle Probe Ø7.5Non-Tapered Pedicle Probe for Screws Ø5.5 and Ø6Pedicle Probe Sharp-BentPedicle Probe Sharp StraightPedicle Probe Blunt-BentPedicle Probe Blunt Straight

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

FDA product codes

CodeNameDevices
HXBPROBE1,109
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT205
HXBProbe175
KAKPROBE, ENT118
MNHOrthosis, Spondylolisthesis Spinal Fixation107
MNIOrthosis, Spinal Pedicle Fixation107

GMDN & GCC registration

  • GMDN code 47862 · non‑implantable
  • Single‑use 5% · sterile 0% · Rx‑only 86% · 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

Outer Diameter (Millimeter) · 31Length (Centimeter) · 26Length (Millimeter) · 12Length (Inch) · 11Angle (degree) · 7

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

How many abdominal/ent/orthopaedic surgical probe, reusable products are registered in the US?

2,356 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Abdominal/ENT/orthopaedic surgical probe, reusable", from 111 companies. The largest labeler is Medtronic Sofamor Danek, Inc. with 12% of records.

Which FDA product codes apply?

HXB (PROBE), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), HXB (Probe), KAK (PROBE, 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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