QuicKlear® C706-1048

by Forestadent Bernhard Förster GmbH

QuicKlear® C706-1048 is a Class II device made by Forestadent Bernhard Förster GmbH, cleared under FDA 510(k) K090933 on 5 Jun 2009 and listed in FDA GUDID since 15 Aug 2019 (UDI-DI EFORC70610481), 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

FDA submission, from GUDID

Trust

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberEFORC70610481 UDI-DI	Date15 Aug 2019Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK090933	Date5 Jun 2009Decided	StatusActive

Official records

FDA 510(k) database 510(k) number K090933

Across registries

2 registries list this device

FDA 510(k) K090933 decided 5 Jun 2009 Active
FDA GUDID UDI-DI EFORC70610481 listed 15 Aug 2019 Listed

Timeline

2 dated events

5 Jun 2009 Cleared FDA 510(k) K090933
15 Aug 2019 Listed FDA GUDID EFORC70610481

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: QuicKlear®
Generic name: Orthodontic bracket, ceramic
Model / reference: C706-1048

Primary DI / UDI-DI: EFORC70610481
510(k) Number: K090933
FDA product code: NJM
GMDN term: Orthodontic bracket, ceramic

Device class: Class II
Regulation number: 872.5470
GUDID distribution status: In Commercial Distribution

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Properties

Single use
Prescription use
Lot / batch number
Manufacturing date

Other properties (11, all answered No)