Medical Device Manufacturer · US , Mchenry , IL

Bausch & Lomb, Inc. - FDA 510(k) Cleared Devices

92 submissions · 92 cleared · Since 1977

Official Website

92

Total

92

Cleared

0

Denied

FDA 510(k) cleared devices by Bausch & Lomb, Inc. Dental ✕

3 devices

1-3 of 3

Cleared Jan 26, 1994

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

Cleared Jun 03, 1992

INTERJET(TM) GINGIVAL CARE INSTRUMENT

Cleared Jul 09, 1991

INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT