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Master-Dent 18-100

by Dentonics, Inc.

Master-Dent 18-100 is a device made by Dentonics, Inc., cleared under FDA 510(k) K823510 on 28 Dec 1982 and listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00816526020404), 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) K823510

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 Number00816526020404 UDI-DI Date16 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK823510 Date28 Dec 1982DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K823510 decided 28 Dec 1982 Active
  • FDA GUDID UDI-DI 00816526020404 listed 16 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K823510
  2. Listed FDA GUDID 00816526020404

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  • Withdrawn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
Dental tooth-etching solution
Model / reference
18-100
Primary DI / UDI-DI
00816526020404
510(k) Number
GMDN term
Dental tooth-etching solution
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental etching solution

Cleared under the same submission (K823510)

and 8 more cleared under K823510

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)