Hydrofera, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Hydrofera, LLC has 7 FDA 510(k) cleared medical devices. Based in Willimantic, US.
Historical record: 7 cleared submissions from 1998 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hydrofera, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hydrofera, LLC
7 devices
Cleared
Nov 06, 2019
Hydrofera Blue READY - Border
General & Plastic Surgery
271d
Cleared
Jan 02, 2014
HYDROFERA BLUE PU BACTERIOSTATIC DRESSING
General & Plastic Surgery
296d
Cleared
Jan 17, 2003
HYDROFERA BACTERIOSTATIC WOUND DRESSING
General & Plastic Surgery
119d
Cleared
Jan 11, 2002
HYDROFERA BACTERIOSTATIC WOUND DRESSING
General & Plastic Surgery
85d
Cleared
Sep 14, 1999
HYDROFERA BACTERISTATIC NASAL DRESSING
Ear, Nose, Throat
362d
Cleared
Mar 02, 1998
HYDROFERA SURGICAL SPEAR
Ophthalmic
105d
Cleared
Feb 13, 1998
HYDROFERA FEMORAL WICK
General & Plastic Surgery
88d