S.P.K. Technology, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What S.P.K. Technology, Inc. makes
S.P.K. Technology, Inc. manufactures titanium and tantalum hemostatic clips designed for surgical use to control bleeding during procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Atrauclip (Titanium Hemostatic Clip) Ref K896997
510(k) 510(k)Atrauclip (Tantalum Hemostatic Clip) Ref K896998
510(k) 510(k)
Frequently asked questions
How many devices does S.P.K. Technology, Inc. have in the registry?
The registry currently lists 2 devices for S.P.K. Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S.P.K. Technology, Inc.'s devices?
Among its 2 most recently registered devices, S.P.K. Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do S.P.K. Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for S.P.K. Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S.P.K. Technology, Inc. in the registry?
The most recently registered devices listed for S.P.K. Technology, Inc. include ATRAUCLIP (TITANIUM HEMOSTATIC CLIP) and ATRAUCLIP (TANTALUM HEMOSTATIC CLIP).