Company · US

Delaware Prosthetics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1983. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GBI	Material, External Aesthetic Restoration, Used With Adhesive	3
FWP	Prosthesis, Chin, Internal	1

Decided	510(k)	Device and applicant	Code
Dec 19, 1983	K832151	PDM SILOXANE PROSTHETIC ORBIT Delaware Prosthetics, Inc.	GBI
Dec 9, 1983	K832153	PDM SILOXANE PROSTHETIC NOSE Delaware Prosthetics, Inc.	GBI
Dec 9, 1983	K832152	PDM SILOXANE PROSTHETIC EAR Delaware Prosthetics, Inc.	GBI
Nov 28, 1983	K832149	PDM SILOXANE PROSTHETIC OBTURATOR Delaware Prosthetics, Inc.
Nov 28, 1983	K832148	PDM SILOXANE PROSTHETIC CHIN IMPLANT Delaware Prosthetics, Inc.	FWP

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.