Consulting Wallah › Device Explorer › Other devices › Arthroscopic obturator
Device Explorer · FDA GUDID · GMDN 58753

Arthroscopic obturator

A non-sterile, hand-held manual surgical instrument designed to fill the lumen of an arthroscopic sleeve (not included) to facilitate insertion of the sleeve into a joint (e.g., shoulder, knee) during arthroscopic examination or surgery. It is typically cannul

US‑registered devices237in commercial distribution
Companies18labelers on GUDID
Single‑use3%of device records
Sterile3%labelled sterile
Prescription75%Rx‑only share
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Share of device records

Smith & Nephew, Inc.5222%
T.A.G Medical Products Agricultural Cooperative Association4619%
Arthrex, Inc.2511%
National Advanced Endoscopy Devices, Inc.2310%
Stryker Corporation219%
Medline Industries, Inc.146%
Biomet Orthopedics, Llc125%
Conmed Corporation125%

Top labelers

CompanyDevicesShare
Smith & Nephew, Inc.5222%
T.A.G Medical Products Agricultural Cooperative Association4619%
Arthrex, Inc.2511%
National Advanced Endoscopy Devices, Inc.2310%
Stryker Corporation219%
Medline Industries, Inc.146%
Biomet Orthopedics, Llc125%
Conmed Corporation125%
Medos International Sàrl104%
Highridge Medical, Llc52%
Integrity Implants Inc.52%
Santa Barbara Imaging Systems, Inc.52%

Company = labeler of record on GUDID. 18 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

KNOTILUS+NAFlareHawkCLEAR-TRACINTELIJETN/ADYONICSAqualocArthrex®No BrandTRUCLEARTMHYDRODAM™ CANNULA SYSTEMHydroDam™ Cannula SystemINNERVUE 2.4MM REUSABLE CANNULAAQUALOC®MAXFIRE CANNULA OBTURATOR FOR

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

FDA product codes

CodeNameDevices
NBHACCESSORIES,ARTHROSCOPIC110
LXHOrthopedic Manual Surgical Instrument53
NBHAccessories, arthroscopic45
NBHAccessories, Arthroscopic22
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT17
LXHOrthopedic manual surgical instrument11

GMDN & GCC registration

  • GMDN code 58753 · non‑implantable
  • Single‑use 3% · sterile 3% · Rx‑only 75% · 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) · 11Length (Millimeter) · 7Lumen/Inner Diameter (Millimeter) · 1

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

How many arthroscopic obturator products are registered in the US?

237 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Arthroscopic obturator", from 18 companies. The largest labeler is Smith & Nephew, Inc. with 22% of records.

Which FDA product codes apply?

NBH (ACCESSORIES,ARTHROSCOPIC), LXH (Orthopedic Manual Surgical Instrument), NBH (Accessories, arthroscopic), NBH (Accessories, Arthroscopic)

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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