Estech, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What Estech, Inc. makes
Estech, Inc. manufactures surgical devices including the COBRA ADHERE SURGICAL SYSTEM, COBRA SURGICAL SYSTEM, ESTECH COBRA(R) GENESIS BIPOLAR CLAMP, ESTECH CLEARVIEW MV ATRIAL DEPRESSOR, and various perfusion cannulas such as the REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA and ESTECH ARTERIAL REMOTE ACCESS PERFUSION CANNULA.
The company's devices are listed in the FDA 510(k) registry and are classified as Class II medical devices. Estech, Inc. is based in the US.
Catalogue
Cobra Adhere Surgical System Ref K041599
510(k) 510(k)- 510(k) 510(k)
- 510(k) 510(k)
Estech Cobra(R) Genesis Bipolar Clamp Ref K133017
510(k) 510(k)Estech Arterial Remote Access Perfusion Cannula Ref K990573
510(k) 510(k)Estech Clearview Mv Atrial Depressor Ref K053021
510(k) 510(k)Cobra Surgical System Ref K051749
510(k) 510(k)
Frequently asked questions
How many devices does Estech, Inc. have in the registry?
The registry currently lists 7 devices for Estech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Estech, Inc.'s devices?
Among its 7 most recently registered devices, Estech, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Estech, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Estech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Estech, Inc. in the registry?
The most recently registered devices listed for Estech, Inc. include COBRA ADHERE SURGICAL SYSTEM, REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA, REMOTE ACCESS PERFUSION CANNULA LEFT AXILLARY 21 FRENCH and ESTECH COBRA(R) GENESIS BIPOLAR CLAMP.