Technimeca Medic, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Technimeca Medic, Inc. makes
Technimeca Medic, Inc. manufactures TECHNOFIL and TECHFIL, which are medical devices designed for specific surgical or procedural applications, though exact uses are not specified.
These devices fall under Class II classification in the US and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Frequently asked questions
How many devices does Technimeca Medic, Inc. have in the registry?
The registry currently lists 2 devices for Technimeca Medic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Technimeca Medic, Inc.'s devices?
Among its 2 most recently registered devices, Technimeca Medic, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Technimeca Medic, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Technimeca Medic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Technimeca Medic, Inc. in the registry?
The most recently registered devices listed for Technimeca Medic, Inc. include TECHNOFIL and TECHFIL.