Instranetics, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Instranetics, Inc. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1977 to 1983. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Instranetics, Inc. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Jan 07, 1983
INSTRA-SAFE
General & Plastic Surgery
52d
Cleared
Jul 20, 1981
TIP-VU
General & Plastic Surgery
21d
Cleared
Jul 20, 1981
SHARPS CADDY FB
General & Plastic Surgery
21d
Cleared
Jul 20, 1981
CAUTERY CADDY PAD
General & Plastic Surgery
21d
Cleared
Feb 26, 1981
LINE CADDY
Orthopedic
22d
Cleared
Feb 12, 1981
BLADE SAFE
General Hospital
17d
Cleared
Dec 18, 1980
SAFE T COUNT
General & Plastic Surgery
36d
Cleared
Nov 17, 1980
SHARPS CADDY MAGNETIC & SHARPS CADDY FOA
General & Plastic Surgery
5d
Cleared
Dec 04, 1978
DISPOSABLE LYMPHANGIOGRAM SET
Radiology
81d
Cleared
Jun 20, 1977
NEURO-SORB PATTIES
Neurology
35d