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Action® Positioner

by Action Products, Inc. 37 variants

Action® Positioner (40718LP-2) is a Class I device made by Action Products, Inc., listed in FDA GUDID since 14 Jan 2021 (UDI-DI 00089904001641), 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 Number00089904001641 UDI-DI Date14 Jan 2021ListedStatusListed 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  • Withdrawn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
Freestanding patient positioner, reusable
Model / Ref / Catalog
Positioner, 40718LP-2
Primary DI / UDI-DI
00089904001641
FDA product code
FMP
GMDN term
Freestanding patient positioner, reusable
Device class
Class I
Regulation number
880.6450
GUDID distribution status
In Commercial Distribution

Related devices

Category: Freestanding patient positioner, reusable

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)