Woodbine Optical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Woodbine Optical Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Woodbine Optical Corp. has 5 FDA 510(k) cleared medical devices. Based in Sharon, US.
Historical record: 5 cleared submissions from 1994 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Woodbine Optical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Woodbine Optical Corp.
5 devices
Cleared
Jun 10, 1997
SOLOS 10MM OPERATING LAPAROSCOPE
General & Plastic Surgery
90d
Cleared
Jan 28, 1997
SOLOS, CIDEO CAMERA REPLACEMENT CABLE, 800/900 SERIES
General & Plastic Surgery
21d
Cleared
Sep 22, 1995
WOODBINE/SOLOS, HIGH RESOLUTION 3-CHIP SURGICAL CAMERA
General & Plastic Surgery
81d
Cleared
Jun 16, 1995
WOODBINE/SOLOS VCM-3, HIGH RESOLUTION ONE-CHIP SURGICAL CAMERA
General & Plastic Surgery
74d
Cleared
Jun 10, 1994
ACCESSORIES, SURGICAL CAMERA
General & Plastic Surgery
98d