Medi-Dyne, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Medi-Dyne, Inc. makes
Medi-Dyne, Inc. makes medical devices such as angiographic catheters, guiding catheters, and modified luer devices. These products are used in medical procedures, specifically in angiography. The company's devices include the MEDI-DYNE ANGIOGRAPHIC CATHETER and the MEDI-DYNE GUIDING CATHETER.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. Medi-Dyne, Inc. is based in the US.
Catalogue
Medi-Dyne Angiographic Catheter Ref K930694
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Modified Luer Ref K931833
Regimes: 510(k) Registry: 510(k)Medi-Dyne Guiding Catheter Ref K970401
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medi-Dyne, Inc. have in the registry?
The registry currently lists 4 devices for Medi-Dyne, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medi-Dyne, Inc.'s devices?
Among its 4 most recently registered devices, Medi-Dyne, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Medi-Dyne, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medi-Dyne, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medi-Dyne, Inc. in the registry?
The most recently registered devices listed for Medi-Dyne, Inc. include MEDI-DYNE ANGIOGRAPHIC CATHETER, 4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER, MODIFIED LUER and MEDI-DYNE GUIDING CATHETER.