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Conmed LG1050

by Conmed Corporation

Conmed LG1050 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K901035 on 23 Apr 1990 and listed in FDA GUDID since 24 Mar 2026 (UDI-DI 10845854040379), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K901035

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10845854040379 UDI-DI Date24 Mar 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK901035 Date23 Apr 1990DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K901035 decided 23 Apr 1990 Active
  • FDA GUDID UDI-DI 10845854040379 listed 24 Mar 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K901035
  2. Listed FDA GUDID 10845854040379

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Conmed
Generic name
Fibreoptic light cable, reusable
Model / Ref / Catalog
LG1050
Primary DI / UDI-DI
10845854040379
510(k) Number
FDA product code
FST
GMDN term
Fibreoptic light cable, reusable
Device class
Class II
Regulation number
878.4580
GUDID distribution status
In Commercial Distribution
Size
Width — 5 Millimeter
Length — 3 Meter

Related devices

Cleared under the same submission (K901035)

and 8 more cleared under K901035

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)