Safeop Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 23
What Safeop Surgical, Inc. makes
Safeop Surgical, Inc. manufactures the EPAD and the EPAD 2 System, which are surgical devices designed for specific intraoperative applications in orthopedic and trauma procedures. These products are intended to assist in the reduction and stabilization of fractures during surgical interventions.
The company’s devices are classified under Class II by the FDA and are listed via the 510(k) pathway. The portfolio is regulated under US medical device laws, and the manufacturer is based in the United States.
Catalogue
Search and filter all 23 devicesCompany details
- DUNS number
- 078641162
- [email protected]
- Phone
- 4107739601
Frequently asked questions
How many devices does Safeop Surgical, Inc. have in the registry?
The registry currently lists 23 devices for Safeop Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safeop Surgical, Inc.'s devices?
Among its 23 most recently registered devices, Safeop Surgical, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (21 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Safeop Surgical, Inc.'s devices fall under?
Among its 23 most recently registered devices, the classes recorded for Safeop Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Safeop Surgical, Inc. in the registry?
The most recently registered devices listed for Safeop Surgical, Inc. include EPAD and The EPAD 2 System.