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Action® OR Table Replacement Pad

by Action Products, Inc. 318 variants

Action® OR Table Replacement Pad (51941A) is a Class I device made by Action Products, Inc., listed in FDA GUDID since 14 Oct 2026 (UDI-DI 00089904011510), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00089904011510 UDI-DI Date14 Oct 2026ListedStatusListed 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  • Withdrawn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
Action®
Generic name
Operating table patient pressure distribution pad, reusable
Model / Ref / Catalog
OR Table Replacement Pad, 51941A
Primary DI / UDI-DI
00089904011510
FDA product code
FMP
GMDN term
Operating table patient pressure distribution pad, reusable
Device class
Class I
Regulation number
880.6450
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FMP (Protector, Skin Pressure).

Other devices from Action Products, Inc.

See all devices from Action Products, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)