Normed Medizin-Technik GmbH is one of 18463 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Normed Medizin-Technik GmbH - FDA 510(k) Cleared Devices
Recent clearances: RECON system - Compression Screws, Tenodesis screw system, RECON system- Grubber Lapidus-, Platar Lapidus-, Tarsalis Plates and Screws
9
Total
9
Cleared
0
Denied
Normed Medizin-Technik GmbH has 9 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 9 cleared submissions from 1994 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Normed Medizin-Technik GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Normed Medizin-Technik GmbH
9 devices
Cleared
Mar 02, 2016
RECON system - Compression Screws
Orthopedic
252d
Cleared
Jan 26, 2016
Tenodesis screw system
Orthopedic
216d
Cleared
Nov 05, 2015
RECON system- Grubber Lapidus-, Platar Lapidus-, Tarsalis Plates and Screws
Orthopedic
87d
Cleared
Oct 30, 2015
RECON system-V-TEK-IVP Plates and Screws
Orthopedic
74d
Cleared
Sep 16, 2015
RECON system - MPJ-Plates
Orthopedic
44d
Cleared
Aug 12, 2015
RECON system
Orthopedic
78d
Cleared
Dec 13, 2013
NORMED PELLEGRIN CALCANEUS STOP SCREW
Orthopedic
77d
Cleared
Aug 02, 2013
NORMED ANKLE FIX SYSTEM 4.0 AND NORMED ANKLE FIX PLUS SYSTEM 4.0
Orthopedic
275d
Cleared
Jul 05, 1994
NORMED TITANIUM MINIPLATE SYSTEM
Dental
463d