FDA 510(k) Searchable Database - Search 175,000+ Clearances

Search 175,000+ FDA 510(k) clearances by K-number, device name, manufacturer or product code. Includes real review time data, denied submission rates and regulatory intelligence not available on any other searchable 510(k) database.

175,972 clearances · 1976 to present · Updated monthly from FDA records

Filters: Dental ×

12,611 results

5569–5592 of 12,611

Search insights Median review: 87d Cleared: 100% Top manufacturer: Dentsply Intl. Lead specialty: Dental

Cleared Dec 22, 2003

Cleared Dec 22, 2003

Kuraray Medical, Inc.

Cleared Dec 22, 2003

Heraeus Kulzer, Inc.

Cleared Dec 19, 2003

IMPAK ACRYLIC REPAIR RESIN LIQUID

Cmp Industries, LLC

Cleared Dec 19, 2003

Eele Laboratories, LLC

Cleared Dec 16, 2003

Reliance Orthodontic Products, Inc.

Cleared Dec 12, 2003

SIROSON L AND SIROSONIC L ULTRASONIC SCALERS

Sirona Dental Systems GmbH

Cleared Dec 10, 2003

A-DEC SELF-CONTAINED WATER SYSTEM, MODEL 0.7 LITER BOTTLE & 2 LITER BOTTLE

Cleared Dec 10, 2003

EMBRACE WETBOND RESTORATION AND PFM REPAIR KIT

Pulpdent Corporation

Cleared Dec 10, 2003

The Clinician'S Preference, LLC

Cleared Dec 10, 2003

IMMEDIATE STABILIZING IMPLANT (ISI)

Cleared Dec 08, 2003

FLUID FILLED TEETHERS

Royal King Infant Products Co. , Ltd.

Cleared Dec 05, 2003

Ivoclar Vivadent, Inc.

Cleared Dec 04, 2003

A-DEC 532/533 DELIVERY SYSTEM MODEL, 532/533

Cleared Dec 04, 2003

BOBCAT PRO SCALER SYSTEM, MODEL G-130

Dentsply International

Cleared Dec 03, 2003

NEWMEDICAL MICRO BONE DISTRACTOR/FIXATOR

Newmedical Technology, Inc.

Cleared Dec 03, 2003

ASEPTICO ENDOPEX V, MODEL AEU-40

Cleared Dec 03, 2003

A-DEC/W&H ELECTRIC MOTOR, MODEL EA-50LT

Cleared Dec 03, 2003

PERMAQUICK SE BONDING SYSTEM

Ultradent Products, Inc.

Cleared Dec 02, 2003

LA500 BLUE LIGHT

Apoza Enterprise Co., Ltd.

Cleared Dec 02, 2003

PFZ PORCELAIN SYSTEM

Cleared Nov 26, 2003

RENOVA INTERNAL HEX IMPLANT SYSTEM

Lifecore Biomedical, Inc.

Cleared Nov 25, 2003

Cleared Nov 25, 2003