Bioenterics Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bioenterics Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Bioenterics Corp. has 4 FDA 510(k) cleared medical devices. Based in Carpinteria, US.
Historical record: 4 cleared submissions from 1992 to 2001. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Bioenterics Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioenterics Corp.
4 devices
Cleared
Jul 09, 2001
GASTRIC SUCTION AND DRAINAGE CATHETER
Gastroenterology & Urology
300d
Cleared
Feb 11, 1997
ENDOLUMINA II TRANSILLUMINATION SYSTEM 56FR E-5630, 50FR E-5030 AND 40FR...
Gastroenterology & Urology
90d
Cleared
Dec 16, 1993
BIOENTERICS ENDOLUMINA ILLUMINATING BOUGIE
Ophthalmic
118d
Cleared
Dec 15, 1992
BIOENTRICS ENDOLUMINA ILLUMINATED BOUGIE
Ophthalmic
84d