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Tokuyama Shield Force

by Tokuyama Dental Corporation

510(k) K100172

Tokuyama Shield Force is a Class II device made by Tokuyama Dental Corporation, cleared under FDA 510(k) K100172 on 21 Oct 2010, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK100172 Date21 Oct 2010ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
LBH
Device class
Class II
Regulation
21 CFR Part 872.3260
Advisory committee
Dental
FDA decision
SESE Substantially Equivalent

Devices cleared under K100172

3 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K100172
UDI-DISize and differences
Tokuyama Shield Force Plus 15111
TOKUYAMA DENTAL CORPORATION
1511104548190151110 —On the market
Tokuyama Shield Force Plus 15121
TOKUYAMA DENTAL CORPORATION
1512104548190151219 —On the market
Tokuyama Shield Force Plus 15141
TOKUYAMA DENTAL CORPORATION
1514104548190151417 —On the market

Similar devices

Other devices filed under FDA product code LBH (Varnish, Cavity).

Other devices from Tokuyama Dental Corporation

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