Premier Medical
United Statesfrom the FDA registration address FDA establishment FEI 2521453
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
What Premier Medical makes
Premier Medical manufactures a biopsy punch for tissue sampling, a die-trak articulator used in dental impression-taking, and a modified decannulation stopper for airway management.
Their portfolio includes Class I and Class II devices, with records of 510(k) submissions in the FDA registry. The company is based in the United States.
Catalogue
Biopsy Punch Ref K896303
Regimes: 510(k) Registry: 510(k)Premier Die-Trak Articulator Ref K884418
Regimes: 510(k) Registry: 510(k)Modified Decannulation Stopper Ref K894050
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 2521453
- Address
- 10090 SANDMEYER LN., PHILADELPHIA, PA, 19116
Frequently asked questions
How many devices does PREMIER MEDICAL have in the registry?
The registry currently lists 3 devices for PREMIER MEDICAL. Devices recorded under merged duplicate company entries are counted once.
Which registries list PREMIER MEDICAL's devices?
Among its 3 most recently registered devices, PREMIER MEDICAL has devices listed in FDA 510(k) (3 devices).
What risk classes do PREMIER MEDICAL's devices fall under?
Among its 3 most recently registered devices, the classes recorded for PREMIER MEDICAL's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from PREMIER MEDICAL in the registry?
The most recently registered devices listed for PREMIER MEDICAL include BIOPSY PUNCH, PREMIER DIE-TRAK ARTICULATOR and MODIFIED DECANNULATION STOPPER.