Tekno Medical Optik-Chirurgie GmbH & Co. is one of 516 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Tekno Medical Optik-Chirurgie GmbH & Co. - FDA 510(k) Cleared Devices
Recent clearances: TEKNO-MEDICAL OBSTETRICAL FORCEPS, INSTRUMENTS FOR LAPAROSCOPY 5 MM, 10 MM WITH COLOURED HANDLE, DETACHABLE ENDODCOPIC INSTRUMENTS 5 MM, 10MM (HANDLE, SHAF
2
Total
2
Cleared
0
Denied
Tekno Medical Optik-Chirurgie GmbH & Co. has 2 FDA 510(k) cleared medical devices. Based in Wurmlingen, DE.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Tekno Medical Optik-Chirurgie GmbH & Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tekno Medical Optik-Chirurgie GmbH & Co.
2 devices