Med-Text Intl.
SwedenFDA applicant, unverified
- Devices
- 1
What Med-Text Intl. makes
Med-Text Intl. manufactures the JAMES TENDOS, a syringe holder designed for medical use.
The JAMES TENDOS is classified as a Class II device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
James Tendos (Syringe Holder) Ref K875297
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med-Text Intl. have in the registry?
The registry currently lists 1 device for Med-Text Intl.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-Text Intl.'s devices?
Among its 1 most recently registered device, Med-Text Intl. has devices listed in FDA 510(k) (1 device).
What risk classes do Med-Text Intl.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Med-Text Intl.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-Text Intl. in the registry?
The most recently registered devices listed for Med-Text Intl. include JAMES TENDOS (SYRINGE HOLDER).