Wilshire Medical Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wilshire Medical Products - FDA 510(k) Cleared Devices
12
Total
8
Cleared
0
Denied
Wilshire Medical Products has 8 FDA 510(k) cleared general & plastic surgery devices. Based in Dallas, US.
Historical record: 8 cleared submissions from 1993 to 1995.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wilshire Medical Products
12 devices
Cleared
Feb 27, 1995
DERMASSIST(TM) HYDROGEL SATURATED GAUZE DRESSING
General & Plastic Surgery
80d
Cleared
Feb 27, 1995
DERMASSIST(TM) HYDROGEL SATURATEED NON WOVEN DRESSING
General & Plastic Surgery
80d
Cleared
Nov 10, 1994
HYDRODERM GEL WOUND DRESSING
General & Plastic Surgery
65d
Cleared
May 20, 1994
DERMAASSIST HYDROCOLLOID DRESSING
General & Plastic Surgery
71d
Cleared
May 20, 1994
HYDRODERM EXTRA THIN INTELLIGENT HYDROCOLLIOID DRESSING
General & Plastic Surgery
67d
Cleared
Apr 14, 1994
DERMASSIST(TM) XEROFORM PETROLATUM DRESSING
General & Plastic Surgery
44d
Cleared
Mar 03, 1994
DERMASSIST PETROLATUM GAUZE,USP
General & Plastic Surgery
64d
Cleared
Mar 03, 1994
DERMASSIST OIL EMULSION NON-ADHERING WOUND DRESSING
General & Plastic Surgery
64d
Cleared
Mar 03, 1994
DERMASSIST WET DRESSING, SALINE
General & Plastic Surgery
57d
Cleared
Mar 03, 1994
DERMASSIST WET DRESSING, WATER
General & Plastic Surgery
56d
Cleared
Feb 02, 1994
HYDRODERM BREATHABLE TRANSPARENT DRESSING
General & Plastic Surgery
57d
Cleared
Feb 03, 1993
DERMASSIST TRANSPARENT SITE DRESSING
General Hospital
163d