Tuttnauer , Ltd. is one of 267 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Tuttnauer , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS, Tuttnauer Horizontal autoclave series model: 4472, 5596, 6690, 66120, T-Edge 10, T-Edge 11
4
Total
4
Cleared
0
Denied
Tuttnauer , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Beit Shemesh, IL.
Last cleared in 2022. Active since 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tuttnauer , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Quarles & Brady as regulatory consultant.
FDA 510(k) Regulatory Record - Tuttnauer , Ltd.
4 devices
Cleared
Dec 16, 2022
Tuttnauer Pre-vacuum Steam Sterilizer models 3870HSG and 3870HSG-WS
General Hospital
109d
Cleared
Sep 20, 2022
Tuttnauer Horizontal autoclave series model: 4472, 5596, 6690, 66120
General Hospital
145d
Cleared
Jan 04, 2022
T-Edge 10, T-Edge 11
General Hospital
103d
Cleared
Jul 08, 2019
Tuttnauer Horizontal Models:4472,5596,6690,66120,69120 and 69180 autoclaves
General Hospital
399d