Skip to content

Pivot Assist Bar 12953

by Dynarex Corp.

Pivot Assist Bar 12953 is a bedrail (FDA Class I; FDA product code FNJ, Bed, Manual) made by Dynarex Corp., listed in FDA GUDID since 9 May 2022 (UDI-DI 00616784295312), 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 Number00616784295312 UDI-DI Date9 May 2022ListedStatusListed 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  • Withdrawn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
Pivot Assist Bar
Generic name
Bedrail
Model / reference
12953
Primary DI / UDI-DI
00616784295312
FDA product code
FNJ
GMDN term
Bedrail
Device class
Class I
Regulation number
880.5120
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FNJ (Bed, Manual).

Other devices from Dynarex Corp.

See all devices from Dynarex Corp. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)