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Master-Dent 32-510

by Dentonics, Inc.

Master-Dent 32-510 is a Class I device made by Dentonics, Inc., cleared under FDA 510(k) K842403 on 17 Aug 1984 and listed in FDA GUDID since 31 Oct 2023 (UDI-DI 00816526022422), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K842403

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816526022422 UDI-DI Date31 Oct 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK842403 Date17 Aug 1984DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K842403 decided 17 Aug 1984 Active
  • FDA GUDID UDI-DI 00816526022422 listed 31 Oct 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K842403
  2. Listed FDA GUDID 00816526022422

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Master-Dent
Generic name
Dentifrice
Model / reference
32-510
Primary DI / UDI-DI
00816526022422
510(k) Number
FDA product code
EJR
GMDN term
Dentifrice
Device class
Class I
Regulation number
872.6030
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dentifrice

Cleared under the same submission (K842403)

and 1 more cleared under K842403

Other devices from Dentonics, Inc.

See all devices from Dentonics, Inc. →

Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)