Dynamedics, Inc.
Country not established
- Devices
- 3
What Dynamedics, Inc. makes
Dynamedics, Inc. manufactures the DYLNAMEDICS A.S.A.P., a device designed for rapid assessment of patient responses, and the DYNAMARK 1000, a system used for monitoring and analyzing physiological data in clinical settings.
The company’s portfolio is regulated under Class II medical devices in the US and includes products listed via the FDA’s 510(k) clearance process. The manufacturer is based in the United States.
Catalogue
Dylnamedics A.S.A.P. Ref K924973
510(k) 510(k)Dynamedics Asar Ref K941083
510(k) 510(k)Dynamark 1000 Ref K873979
510(k) 510(k)
Frequently asked questions
How many devices does Dynamedics, Inc. have in the registry?
The registry currently lists 3 devices for Dynamedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dynamedics, Inc.'s devices?
Among its 3 most recently registered devices, Dynamedics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dynamedics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dynamedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dynamedics, Inc. in the registry?
The most recently registered devices listed for Dynamedics, Inc. include DYLNAMEDICS A.S.A.P., DYNAMEDICS ASAR and DYNAMARK 1000.