Pro-Tronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Pro-Tronics, Inc. makes
Pro-Tronics, Inc. specializes in refurbished C-arm imaging systems, including models such as the General Electric AMX 110, AMX II, and AMX 3. These devices are designed for intraoperative fluoroscopy, enabling real-time X-ray imaging during surgical procedures. The portfolio also includes refurbished Mobil C-arm systems, which support orthopedic and vascular interventions.
The company’s refurbished C-arm systems fall under FDA Class II medical devices and are recorded in the FDA’s 510(k) premarket notification database. These devices are intended for reuse within regulated medical imaging workflows. Pro-Tronics, Inc. is based in the United States.
Catalogue
General Electric Amx 110, Amx Ii And Amx 3 Ref K944442
Regimes: 510(k) Registry: 510(k)Mobil C-Arm, Regurbished, Various Models Ref K950971
Regimes: 510(k) Registry: 510(k)General Electric Amx 110 Ref K891143
Regimes: 510(k) Registry: 510(k)General Electric Amx Ii Ref K891142
Regimes: 510(k) Registry: 510(k)General Electric Amx 3 Ref K902610
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pro-Tronics, Inc. have in the registry?
The registry currently lists 5 devices for Pro-Tronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pro-Tronics, Inc.'s devices?
Among its 5 most recently registered devices, Pro-Tronics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Pro-Tronics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Pro-Tronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pro-Tronics, Inc. in the registry?
The most recently registered devices listed for Pro-Tronics, Inc. include GENERAL ELECTRIC AMX 110, AMX II AND AMX 3, MOBIL C-ARM, REGURBISHED, VARIOUS MODELS, GENERAL ELECTRIC AMX 110 and GENERAL ELECTRIC AMX II.