Heinz Kurz is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Heinz Kurz - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Heinz Kurz has 5 FDA 510(k) cleared medical devices. Based in Amsterdam 1017ap, NL.
Historical record: 5 cleared submissions from 1997 to 2001. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Heinz Kurz Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Heinz Kurz
5 devices
Cleared
Mar 08, 2001
KURZ ANGULAR PISTON-TITANIUM PROSTHESIS, MODELS 1006 600, 1006 601, 1006 602,...
Ear, Nose, Throat
22d
Cleared
May 18, 1999
TITANIUM VOCAL FOLD MEDIALIZING IMPLANT, MODELS 5001 001 (FEMALE), AND 5001...
Ear, Nose, Throat
29d
Cleared
Mar 31, 1999
TUBINGEN TITANIUM PROSTHESIS (TTP) VARIO, MODELS AERIAL 1004 010 & BELL 1002 010
Ear, Nose, Throat
12d
Cleared
Nov 21, 1997
K-PISTON WITH BAND HOOK /ANGULAR PISTON
Ear, Nose, Throat
74d
Cleared
Aug 04, 1997
BELL PROSTHESIS (PARTIAL)
Ear, Nose, Throat
33d