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Operating Room Innovations, Inc OH-4

by Operating Room Innovations, Inc.

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00854150007361 UDI-DI Date23 Sep 2021ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Operating Room Innovations, Inc
Generic Name
Face splash shield, single-use
Model / Ref / Catalog
OH-4
Primary DI / UDI-DI
00854150007361
FDA Product Code
LYU
GMDN Term
Face splash shield, single-use
Device Class
Class I
Regulation Number
878.4040
GUDID distribution status
Not in Commercial Distribution

Other devices from Operating Room Innovations, Inc.

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No