Delaware Prosthetics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Delaware Prosthetics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Delaware Prosthetics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 5 cleared submissions from 1983 to 1983. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Delaware Prosthetics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Delaware Prosthetics, Inc.
5 devices
Cleared
Dec 19, 1983
PDM SILOXANE PROSTHETIC ORBIT
General & Plastic Surgery
167d
Cleared
Dec 09, 1983
PDM SILOXANE PROSTHETIC EAR
General & Plastic Surgery
157d
Cleared
Dec 09, 1983
PDM SILOXANE PROSTHETIC NOSE
General & Plastic Surgery
157d
Cleared
Nov 28, 1983
PDM SILOXANE PROSTHETIC CHIN IMPLANT
General & Plastic Surgery
146d
Cleared
Nov 28, 1983
PDM SILOXANE PROSTHETIC OBTURATOR
General & Plastic Surgery
146d