Prestige Medical
Also registered as Prestige Medical Corp.
United Statesfrom the FDA registration address FDA establishment FEI 2081040
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Prestige Medical Series 2100 Clinical Autoclave Ref K962903
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2081040
- Address
- 2750 113th St, Grand Prairie, TX, 75050
FDA establishments
- Prestige Medical, Ltd. BLACKBURN Lancashire · GB FEI 3008342949
Frequently asked questions
How many devices does Prestige Medical have in the registry?
The registry currently lists 1 device for Prestige Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prestige Medical's devices?
Among its 1 most recently registered device, Prestige Medical has devices listed in FDA 510(k) (1 device).
What risk classes do Prestige Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Prestige Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prestige Medical in the registry?
The most recently registered devices listed for Prestige Medical include PRESTIGE MEDICAL SERIES 2100 CLINICAL AUTOCLAVE.
Which FDA establishments are linked to Prestige Medical?
1 FDA establishment is linked to Prestige Medical in the registry; they are listed on the company page.