Vesitec Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Vesitec Medical, Inc. makes
Vesitec Medical, Inc. manufactures orthopedic surgical instruments, including a drill guide for precise bone preparation, a suture passer for tendon or ligament attachment, and a bone anchor designed for securing soft tissue to bone.
The company’s products are regulated under FDA Class I and Class II classifications, with some devices authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) registry, and the company is based in the United States.
Catalogue
Vesitec Drill Guide Ref K931182
Regimes: 510(k) Registry: 510(k)Vesitec Suture Passer Ref K931181
Regimes: 510(k) Registry: 510(k)Bone Anchor For Soft Tissue Attachment Ref K932925
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Vesitec Medical, Inc. have in the registry?
The registry currently lists 3 devices for Vesitec Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vesitec Medical, Inc.'s devices?
Among its 3 most recently registered devices, Vesitec Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Vesitec Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Vesitec Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Vesitec Medical, Inc. in the registry?
The most recently registered devices listed for Vesitec Medical, Inc. include VESITEC DRILL GUIDE, VESITEC SUTURE PASSER and BONE ANCHOR FOR SOFT TISSUE ATTACHMENT.