Polyganics B.V., is one of 62 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Polyganics B.V., - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Polyganics B.V., has 9 FDA 510(k) cleared medical devices. Based in Groningen, NL.
Historical record: 9 cleared submissions from 2003 to 2014. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Polyganics B.V., Filter by specialty or product code using the sidebar.
Polyganics B.V., — FDA 510(k) Products and Clearance History
9 devices
Cleared
Oct 23, 2014
HEMOPORE
Ear, Nose, Throat
108d
Cleared
Aug 07, 2014
NASOPORE-FD
Ear, Nose, Throat
69d
Cleared
Oct 20, 2011
NEUROLAC(R) NERVE GUIDE
Neurology
73d
Cleared
May 07, 2007
NASOPORE EAR
Ear, Nose, Throat
54d
Cleared
Oct 18, 2006
NASOPORE EAR, MODELS ND04, ND05
Ear, Nose, Throat
49d
Cleared
Nov 21, 2005
NASOPORE NASAL DRESSING, MODEL NDOX-YYY/ZZ
Ear, Nose, Throat
110d
Cleared
May 04, 2005
NEUROLAC NERVE GUIDE
Neurology
58d
Cleared
Nov 08, 2004
VIVOSORB SHEET, MODEL FS01
General & Plastic Surgery
27d
Cleared
Oct 10, 2003
NEUROLAC NERVE GUIDE MODELS NG01-15/03, NG01-020/03, NG01 025/03, NG01-030/03
Neurology
93d