Renaissance Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renaissance Medical, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Renaissance Medical, Inc. has 4 FDA 510(k) cleared medical devices. Based in Dana Point, US.
Historical record: 4 cleared submissions from 1992 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Renaissance Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Renaissance Medical, Inc.
4 devices
Cleared
Jan 18, 1994
WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
General & Plastic Surgery
84d
Cleared
Jan 10, 1994
ROYL-DERM WOUND HYDROGEL DRESSING
General & Plastic Surgery
210d
Cleared
Jan 10, 1994
ROYL-DERM WOUND HYDROGEL STERILE UNIT DOSE
General & Plastic Surgery
159d
Cleared
Oct 28, 1992
ROYL-DERM WOUND HYDROGEL
General & Plastic Surgery
139d