Medron, LLC
United StatesFDA applicant, unverified FDA FEI 1000306216
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medron, LLC makes
Medron, LLC makes medical devices such as vessel dilators, including the MEDRON Vessel Dilator in various sizes, which are made of HDPE.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Injection Cap Ref K940775
Regimes: 510(k) Registry: 510(k)MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator Ref K192283
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000306216
- Address
- 1518 S Gladiola St, SALT LAKE CITY, UT, 84104
Frequently asked questions
How many devices does Medron, LLC have in the registry?
The registry currently lists 3 devices for Medron, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medron, LLC's devices?
Among its 3 most recently registered devices, Medron, LLC has devices listed in FDA 510(k) (3 devices).
What risk classes do Medron, LLC's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medron, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medron, LLC in the registry?
The most recently registered devices listed for Medron, LLC include CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH), INJECTION CAP and MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator.