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AllPro Interdental

by Cordica Medical, Inc. 5 variants

AllPro Interdental (T-5-36) is a Class I device made by Cordica Medical, Inc., listed in FDA GUDID since 27 Jul 2022 (UDI-DI 00813360022045), 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 Number00813360022045 UDI-DI Date27 Jul 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  • Withdrawn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
AllPro
Generic name
Basic manual toothbrush
Model / Ref / Catalog
Interdental, T-5-36
Primary DI / UDI-DI
00813360022045
FDA product code
EFW
GMDN term
Basic manual toothbrush
Device class
Class I
Regulation number
872.6855
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic manual toothbrush

Similar devices

Other devices filed under FDA product code EFW (Toothbrush, Manual).

Other devices from Cordica Medical, Inc.

See all devices from Cordica Medical, Inc. →

Properties

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