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Innomed, Inc. 51617115

by Innomed, Inc.

Innomed, Inc. 51617115 is a Class I device made by Innomed, Inc., listed in FDA GUDID since 14 Oct 2025 (UDI-DI 00840277132888), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00840277132888 UDI-DI Date14 Oct 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Innomed, Inc.
Generic name
Leg procedure positioner
Model / Ref / Catalog
51617115
Primary DI / UDI-DI
00840277132888
FDA product code
KIL
GMDN term
Leg procedure positioner
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code KIL (Positioner, Socket).

Other devices from Innomed, Inc.

See all devices from Innomed, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)