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Device Explorer · FDA GUDID · GMDN 62458

Arthroscopic access cannula, reusable

A single-lumen, surgical device intended to be percutaneously inserted into a joint to create an access port for an arthroscope/arthroscopic instrument during arthroscopy. The cannula is designed to facilitate the passage of surgical instruments while preventi

US‑registered devices350in commercial distribution
Companies19labelers on GUDID
Single‑use2%of device records
Sterile1%labelled sterile
Prescription91%Rx‑only share
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Share of device records

Stryker Corporation7521%
Arthrex, Inc.6218%
Highridge Medical, Llc4513%
Integrity Implants Inc.4312%
Sontec Instruments, Inc.288%
Avalign Technologies, Inc.154%
Depuy Mitek, Llc134%
Tigon Medical Llc123%

Top labelers

CompanyDevicesShare
Stryker Corporation7521%
Arthrex, Inc.6218%
Highridge Medical, Llc4513%
Integrity Implants Inc.4312%
Sontec Instruments, Inc.288%
Avalign Technologies, Inc.154%
Depuy Mitek, Llc134%
Tigon Medical Llc123%
Medos International Sàrl123%
Expanding Innovations, Inc.93%
Conmed Corporation93%
Karl Storz Gmbh & Co. Kg72%

Company = labeler of record on GUDID. 19 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

FlowPortSharpShooterNASpeed-LockENDOCAMELEONn.a.FlareHawkCLEAR-TRAC2.9 JuggerKnot Self-Punching Cannula2.9 JuggerKnot Self-Punching ObturatorArthrex®CANNULA STRAIGHTCANNULA UPCANNULA CURVEDCannulaTigon Medical

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

FDA product codes

CodeNameDevices
NBHAccessories, arthroscopic103
LXHOrthopedic manual surgical instrument92
LXHOrthopedic Manual Surgical Instrument63
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT35
NBHACCESSORIES,ARTHROSCOPIC24
FSMTRAY, SURGICAL, INSTRUMENT18

GMDN & GCC registration

  • GMDN code 62458 · non‑implantable
  • Single‑use 2% · sterile 1% · Rx‑only 91% · 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) · 30Length (Millimeter) · 21Length (Inch) · 1Length (Centimeter) · 1

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

How many arthroscopic access cannula, reusable products are registered in the US?

350 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic access cannula, reusable", from 19 companies. The largest labeler is Stryker Corporation with 21% of records.

Which FDA product codes apply?

NBH (Accessories, arthroscopic), LXH (Orthopedic manual surgical instrument), LXH (Orthopedic Manual Surgical Instrument), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT)

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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