Piezosurgery S.r.l.
ItalyFDA applicant, unverified
- Devices
- 4
What Piezosurgery S.r.l. makes
Piezosurgery S.R.L. manufactures piezoelectric surgical devices designed for precision bone cutting and tissue separation in medical procedures. These include standalone piezoelectric systems and integrated solutions like the OSSTEM PIEZO series, which utilise ultrasonic vibrations for controlled surgical interventions.
The company’s piezoelectric devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. These products are intended for use in the United States, where they are subject to FDA oversight.
Catalogue
Piezosurgery Ref K052518
Regimes: 510(k) Registry: 510(k)Piezosurgery Device Ref K043408
Regimes: 510(k) Registry: 510(k)Piezosurgery Medical Ref K083284
Regimes: 510(k) Registry: 510(k)Piezosurgery 3; Osstem Piezo Ref K091227
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Piezosurgery S.R.L. have in the registry?
The registry currently lists 4 devices for Piezosurgery S.R.L.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Piezosurgery S.R.L.'s devices?
Among its 4 most recently registered devices, Piezosurgery S.R.L. has devices listed in FDA 510(k) (4 devices).
What risk classes do Piezosurgery S.R.L.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Piezosurgery S.R.L.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Piezosurgery S.R.L. in the registry?
The most recently registered devices listed for Piezosurgery S.R.L. include PIEZOSURGERY, PIEZOSURGERY DEVICE, PIEZOSURGERY MEDICAL and PIEZOSURGERY 3; OSSTEM PIEZO.