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Innomed, Inc. 1825-01

by Innomed, Inc.

Innomed, Inc. 1825-01 is a Class I device made by Innomed, Inc., listed in FDA GUDID since 26 May 2020 (UDI-DI 00840277102218), 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 Number00840277102218 UDI-DI Date26 May 2020ListedStatusListed 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  • Withdrawn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
Orthopaedic surgical distractor, external
Model / Ref / Catalog
1825-01
Primary DI / UDI-DI
00840277102218
FDA product code
LXH
GMDN term
Orthopaedic surgical distractor, external
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic surgical distractor, external

Similar devices

Other devices filed under FDA product code LXH (Orthopedic Manual Surgical Instrument).

Other devices from Innomed, Inc.

See all devices from Innomed, Inc. →

Properties

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