Skip to content

Tcc-Ez® TCC23001

by Acell, Inc.

Tcc-Ez® TCC23001 is a Class I device made by Acell, Inc., listed in FDA GUDID since 20 Aug 2026 (UDI-DI 10381780541165), 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 Number10381780541165 UDI-DI Date20 Aug 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  • Withdrawn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
Tcc-Ez®
Generic name
Cast boot
Model / Ref / Catalog
TCC23001
Primary DI / UDI-DI
10381780541165
FDA product code
ITG
GMDN term
Cast boot
Device class
Class I
Regulation number
890.3025
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code ITG (BANDAGE, CAST).

Other devices from Acell, Inc.

See all devices from Acell, Inc. →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)