Hermitage Hospital Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hermitage Hospital Products, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Hermitage Hospital Products, Inc. has 8 FDA 510(k) cleared medical devices. Based in Niantic, US.
Historical record: 8 cleared submissions from 1982 to 1995. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hermitage Hospital Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hermitage Hospital Products, Inc.
8 devices
Cleared
May 03, 1995
OR TOWEL
General Hospital
386d
Cleared
Nov 23, 1992
CLINISORB
General & Plastic Surgery
151d
Cleared
Oct 06, 1992
COMBINE II WETPROOF PAD
General & Plastic Surgery
103d
Cleared
Apr 27, 1989
HERMITEX SPONGE
General & Plastic Surgery
45d
Cleared
Oct 14, 1986
SPONGES STERILE TWIN PAKT AND SINGLES
General & Plastic Surgery
21d
Cleared
Nov 07, 1984
CUSTOM BURN DRESSING KIT
General & Plastic Surgery
41d
Cleared
Nov 05, 1982
DRESSING SPONGE
General & Plastic Surgery
24d
Cleared
Oct 13, 1982
LAPAROTOMY SPONGE
General & Plastic Surgery
44d