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Rexall 10686401

by Dolgencorp, LLC

Rexall 10686401 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 9 Nov 2020 (UDI-DI 00850019681857), 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 Number00850019681857 UDI-DI Date9 Nov 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  • Withdrawn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
Rexall
Generic name
Periodontal hoe
Model / reference
10686401
Primary DI / UDI-DI
00850019681857
FDA product code
EAX, EMQ
GMDN term
Periodontal hoe
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental mirror, reusablePeriodontal hoe

Other devices from Dolgencorp, LLC

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Properties

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