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Device Explorer · FDA GUDID · GMDN 37089

Light source adaptor

A small connecting device designed to permit the connection of the devices that together deliver light to a work field from a light source. This device is used to connect together products of dissimilar manufacture and dimensions, e.g., a fibreoptic light cabl

US‑registered devices733in commercial distribution
Companies39labelers on GUDID
Single‑use2%of device records
Sterile1%labelled sterile
Prescription24%Rx‑only share
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Share of device records

Aspen Surgical Products, Inc.50869%
Karl Storz Gmbh & Co. Kg405%
Depuy Spine, Llc162%
Richard Wolf Gmbh142%
Fentex Medical Gmbh132%
Innomed, Inc.101%
Stryker Corporation91%
Schölly Fiberoptic Gmbh91%

Top labelers

CompanyDevicesShare
Aspen Surgical Products, Inc.50869%
Karl Storz Gmbh & Co. Kg405%
Depuy Spine, Llc162%
Richard Wolf Gmbh142%
Fentex Medical Gmbh132%
Innomed, Inc.101%
Stryker Corporation91%
Schölly Fiberoptic Gmbh91%
Olympus Winter & Ibe Gmbh91%
Hayden Medical, Inc.91%
Medos International Sàrl71%
Globus Medical, Inc.61%

Company = labeler of record on GUDID. 39 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NASafeLightPENTAXLight Guide AdapterLight guide adapterUniversal Light Guide AdapterPENTAX MedicalFENTEXAdapterFUSION DESIGNRZ Medizintechnik GmbHn.a.OlympusN/AAspen® Flexible Light Handle AdapterAspen® Rigid Light Handle Adapter

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

FDA product codes

CodeNameDevices
FTALight, surgical, accessories520
FCWLight source, fiberoptic, routine56
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT25
FDSGastroscope and accessories, flexible/rigid15
FEMACCESSORIES, PHOTOGRAPHIC, FOR ENDOSCOPE (EXCLUDE LIGHT SOUR15
EQHSOURCE, CARRIER, FIBEROPTIC LIGHT13

GMDN & GCC registration

  • GMDN code 37089 · non‑implantable
  • Single‑use 2% · sterile 1% · Rx‑only 24% · OTC 1%
  • 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) · 2Length (Millimeter) · 2

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

How many light source adaptor products are registered in the US?

733 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Light source adaptor", from 39 companies. The largest labeler is Aspen Surgical Products, Inc. with 69% of records.

Which FDA product codes apply?

FTA (Light, surgical, accessories), FCW (Light source, fiberoptic, routine), LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT), FDS (Gastroscope and accessories, flexible/rigid)

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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