Mpm Medical., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mpm Medical., Inc. - FDA 510(k) Cleared Devices
9
Total
8
Cleared
0
Denied
Mpm Medical., Inc. has 8 FDA 510(k) cleared medical devices. Based in Fort Worth, US.
Historical record: 8 cleared submissions from 1993 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mpm Medical., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mpm Medical., Inc.
9 devices
Cleared
May 10, 2006
ORAMAGIC PLUS ORAL WOUND RINSE
General & Plastic Surgery
89d
Cleared
Mar 14, 2003
ORAMAGICRX ORAL WOUND RINSE
General & Plastic Surgery
86d
Cleared
Nov 01, 2002
REGENECARE WOUND GEL
General & Plastic Surgery
255d
Cleared
Dec 23, 1999
MPM REGENECARE WOUND GEL
General & Plastic Surgery
188d
Cleared
Jun 26, 1996
MPM HYDROGEL DRESSING (NON-STERILE)
General & Plastic Surgery
22d
Cleared
Jun 30, 1995
MPM HYDROGEL DRESSING
General & Plastic Surgery
46d
Cleared
Jul 11, 1994
MPM HYDROGEL
General & Plastic Surgery
26d
Cleared
Jul 08, 1993
MPM HYDROGEL SATURATED DRESSING
General & Plastic Surgery
155d
Cleared
Apr 08, 1993
MPM WET DRESSING (SALINE)
General & Plastic Surgery
128d