Oral-B Laboratories is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Oral-B Laboratories - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Oral-B Laboratories has 8 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 8 cleared submissions from 1988 to 1995. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Oral-B Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Oral-B Laboratories
8 devices
Cleared
Apr 27, 1995
ORAL-B INTERDENTAL WOODSTICKS WITH FLUORIDE
Dental
328d
Cleared
Apr 27, 1995
ORAL-B ULTRAFLOSS WITH FLLUORIDE
Dental
300d
Cleared
Sep 09, 1994
ORAL-B PERIOFLEX SUBGINGIVAL IRRIGATOR
Dental
70d
Cleared
Sep 29, 1993
ORAL-B DISPOSABLE PROPHY ANGLE W/PROPHY CUP
Dental
103d
Cleared
Jan 28, 1993
ORAL-B DENTAL TAPE WITH FLUORIDE
Dental
94d
Cleared
Jan 28, 1993
ORAL-B DENTAL FLOSS WITH FLUORIDE
Dental
94d
Cleared
Sep 30, 1991
FIBRETWINS
Gastroenterology & Urology
47d
Cleared
Aug 26, 1988
ORAL-B FLOSSERS
Dental
38d