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Master-Dent 32-500

by Dentonics, Inc.

Master-Dent 32-500 is a Class I device made by Dentonics, Inc., cleared under FDA 510(k) K873686 on 12 Nov 1987 and listed in FDA GUDID since 26 Oct 2023 (UDI-DI 00816526022415), 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) K873686

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 Number00816526022415 UDI-DI Date26 Oct 2023ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK873686 Date12 Nov 1987DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K873686 decided 12 Nov 1987 Active
  • FDA GUDID UDI-DI 00816526022415 listed 26 Oct 2023 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K873686
  2. Listed FDA GUDID 00816526022415

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  • Withdrawn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
32-500
Primary DI / UDI-DI
00816526022415
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 (K873686)

Similar devices in this category

Other devices filed under Dentifrice.

Other devices from Dentonics, Inc.

See all devices from Dentonics, Inc. →

Properties

  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)