Medline Renewal
United Statesfrom the FDA registration address FDA FEI 3002299608
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medline Renewal makes
Medline Renewal manufactures reprocessed sinus application blades, specifically the Gyrus-Diego model, designed for surgical sinus procedures.
These devices are classified as Class I under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3002299608
- Address
- 1500 NE Hemlock Avenue, Redmond, OR, 97756
Frequently asked questions
How many devices does Medline Renewal have in the registry?
The registry currently lists 1 device for Medline Renewal. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medline Renewal's devices?
Among its 1 most recently registered device, Medline Renewal has devices listed in FDA 510(k) (1 device).
What risk classes do Medline Renewal's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medline Renewal's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Medline Renewal in the registry?
The most recently registered devices listed for Medline Renewal include MEDLINE RENEWAL REPROCESSED GYRUS-DIEGO SINUS APPLICATION BLADES.