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Rexall 31030001

by Dolgencorp, LLC

Rexall 31030001 is a Class I device made by Dolgencorp, LLC, listed in FDA GUDID since 17 Dec 2021 (UDI-DI 00850032682442), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850032682442 UDI-DI Date17 Dec 2021ListedStatusListed 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  • Withdrawn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
Dental floss
Model / reference
31030001
Primary DI / UDI-DI
00850032682442
FDA product code
JES
GMDN term
Dental floss
Device class
Class I
Regulation number
872.6390
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JES (Floss, Dental).

Other devices from Dolgencorp, LLC

See all devices from Dolgencorp, LLC →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (10, all answered No)