Penn Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Devine (Suprapubic Sound And Guide) Ref K873177
Regimes: 510(k) Registry: 510(k)Rorertazzi Nasopharyngeal Airway Ref K873949
Regimes: 510(k) Registry: 510(k)Ureteral Bulb Dilators Ref K873178
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Huffman Biopsy Unit Ref K873176
Regimes: 510(k) Registry: 510(k)Penn 3-Ring Handle Ref K862729
Regimes: 510(k) Registry: 510(k)Gastrointestinal Tube Ref K870508
Regimes: 510(k) Registry: 510(k)Ureteral Stent Ref K871667
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penn Medical Devices, Inc. have in the registry?
The registry currently lists 8 devices for Penn Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penn Medical Devices, Inc.'s devices?
Among its 8 most recently registered devices, Penn Medical Devices, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Penn Medical Devices, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Penn Medical Devices, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Penn Medical Devices, Inc. in the registry?
The most recently registered devices listed for Penn Medical Devices, Inc. include DEVINE (SUPRAPUBIC SOUND AND GUIDE), RORERTAZZI NASOPHARYNGEAL AIRWAY, URETERAL BULB DILATORS and PENN & OLYMPUS URETEROSCOPY GUIDE SHEATH & DILATOR.