Skip to content

Operon Oz 7552075

by STRYKER Communications, Inc.

Operon Oz 7552075 is a Class I device made by STRYKER Communications, Inc., listed in FDA GUDID since 24 Jan 2019 (UDI-DI 07613327395037), 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 Number07613327395037 UDI-DI Date24 Jan 2019ListedStatusListed 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  • Withdrawn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
Operon
Generic name
Operating table mattress, basic
Model / Ref / Catalog
OZ 7552075
Primary DI / UDI-DI
07613327395037
FDA product code
LWG
GMDN term
Operating table mattress, basic
Device class
Class I
Regulation number
878.4950
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LWG (SURGICAL TABLE CUSHION).

Other devices from STRYKER Communications, Inc.

See all devices from STRYKER Communications, Inc. →

Properties

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