Product code EEG— Dental

FDA has cleared 12 devices under product code EEG between 1979 and 2012, filed by 12 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 20122 clearances
• 20071 clearance
• 20051 clearance
• 20042 clearances
• 19901 clearance
• 19891 clearance
• 19862 clearances
• 19831 clearance
• 19791 clearance

• Union Broach, Div. Moyco Industries, Inc.1 clearance
• Syneron Beauty1 clearance
• Reynolds Laboratories1 clearance
• Henry Schein, Inc.1 clearance
• Grass-Telefactor Product Group1 clearance
• Dr. Fresh, Inc.1 clearance
• Dentovations, Inc.1 clearance
• Cosmetic Dental Materials, Inc.1 clearance
• CAO Group, Inc.1 clearance
• Beks Incorporated1 clearance

• K122725 — TANDA PEARL, ULTRAWYTE, PEARLSyneron Beauty·2012-11-27
• K110888 — ABSOLUTE WHITE LIGHTDr. Fresh, Inc.·2012-01-12
• K063704 — BRITEWHITE TEETH WHITENING SYSTEM, MODEL BW1101Beks Incorporated·2007-02-20
• K052040 — QUICKSMILECosmetic Dental Materials, Inc.·2005-10-18
• K041392 — SONX 35 ULTRASONIC BLEACHING SYSTEM; SONIWHITE ULTRA SONIC, MODEL QUICK WHITE USCAO Group, Inc.·2004-11-08
• K042153 — SOUTH BEACH SMILE LIGHT WHITENING SYSTEMDentovations, Inc.·2004-11-08
• K895174 — UNION BROACH BLEACHING LIGHTUnion Broach, Div. Moyco Industries, Inc.·1990-04-13
• K884937 — BEEHIVE-64 OR BEEHIVE-32, DIGITAL EEG RECORDINGGrass-Telefactor Product Group·1989-04-14
• K862385 — SCHEIN BLEACHING UNITHenry Schein, Inc.·1986-10-30
• K854692 — MONARCH II BLEACHING INSTRUMENTAlmore Intl., Inc.·1986-05-12
• K832179 — HOT PROBE MODEL 6001Analytic Technology·1983-10-04
• K790378 — REYNOLDS BLEACHING PROCESSReynolds Laboratories·1979-04-10