Skip to content

Medline FCE1232TPZ

by Medline Industries, Inc.

Medline FCE1232TPZ is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 13 Oct 2020 (UDI-DI 40080196326151), 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 Number40080196326151 UDI-DI Date13 Oct 2020ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Trapeze bar exerciser
Model / Ref / Catalog
FCE1232TPZ
Primary DI / UDI-DI
40080196326151
FDA product code
FNL
GMDN term
Trapeze bar exerciser
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FNL (BED, AC-POWERED ADJUSTABLE HOSPITAL).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (11, all answered No)