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AllPro 211 (Screw)

by Cordica Medical, Inc. 3 variants

AllPro 211 (Screw) (211-12) is a Class I device made by Cordica Medical, Inc., listed in FDA GUDID since 25 Jul 2023 (UDI-DI 00813360023523), 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 Number00813360023523 UDI-DI Date25 Jul 2023ListedStatusListed 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  • Withdrawn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
Dental polishing cup, single-use
Model / Ref / Catalog
211 (Screw), 211-12
Description
Prophy Brush, Metal, Screw, tapered, White Nylon
Primary DI / UDI-DI
00813360023523
FDA product code
EHK
GMDN term
Dental polishing cup, single-use
Device class
Class I
Regulation number
872.6290
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental polishing cup, single-use

Similar devices

Other devices filed under FDA product code EHK (Cup, Prophylaxis).

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)