Synthemed Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Synthemed Corp. makes
Synthemed Corp. manufactures medical devices including the SYNTHEMED DEVICE, a general-purpose product, and the SYNTHEMED PULSE GENERATOR VVI MODEL 1000, a pacemaker designed for ventricular demand pacing.
The company’s portfolio includes Class I and Class III devices, all of which are recorded in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Synthemed Device Ref K082276
510(k) 510(k)Synthemed Pulse Generator Vvi Model 1000 Ref K812464
510(k) 510(k)
Frequently asked questions
How many devices does Synthemed Corp. have in the registry?
The registry currently lists 2 devices for Synthemed Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synthemed Corp.'s devices?
Among its 2 most recently registered devices, Synthemed Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Synthemed Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Synthemed Corp.'s devices are Class I and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Synthemed Corp. in the registry?
The most recently registered devices listed for Synthemed Corp. include SYNTHEMED DEVICE and SYNTHEMED PULSE GENERATOR VVI MODEL 1000.