Innomed, Inc. 5071

by Innomed, Inc.

Innomed, Inc. 5071 is a Class I device made by Innomed, Inc., listed in FDA GUDID since 8 Dec 2020 (UDI-DI 00840277120946), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00840277120946 UDI-DI	Date8 Dec 2020Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00840277120946

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Innomed, Inc.
Generic name: Hand-held surgical retractor, reusable
Model / Ref / Catalog: 5071

Primary DI / UDI-DI: 00840277120946
FDA product code: LXH
GMDN term: Hand-held surgical retractor, reusable

Device class: Class I
Regulation number: 888.4540
GUDID distribution status: In Commercial Distribution

Sterilisation method: Moist Heat or Steam Sterilization

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Other devices filed under Hand-held surgical retractor, reusable.

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Properties

Sterilise before use
Premarket exempt

Other properties (13, all answered No)