All-Pro Imaging Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What All-Pro Imaging Corp. makes
All-Pro Imaging Corp. manufactures medical imaging devices, including the ALL-PRO 100, MEDSCOPE, ALL-PRO 2010, and the AII-PRO 100 PLUS and ALL-PRO 200 series. These products are designed for diagnostic imaging applications, likely covering modalities such as fluoroscopy, endoscopy, or portable X-ray systems.
The company’s portfolio consists of Class II medical devices, each authorised through the FDA’s 510(k) clearance process. These devices are listed under U.S. regulatory requirements and are intended for commercial distribution within the United States.
Catalogue
All-Pro 100 Ref K911291
Regimes: 510(k) Registry: 510(k)Medscope Ref K001314
Regimes: 510(k) Registry: 510(k)All-Pro 2010 Ref K001321
Regimes: 510(k) Registry: 510(k)Aii-Pro 100 Plus And All-Pro 200 Ref K991435
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does All-Pro Imaging Corp. have in the registry?
The registry currently lists 4 devices for All-Pro Imaging Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list All-Pro Imaging Corp.'s devices?
Among its 4 most recently registered devices, All-Pro Imaging Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do All-Pro Imaging Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for All-Pro Imaging Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from All-Pro Imaging Corp. in the registry?
The most recently registered devices listed for All-Pro Imaging Corp. include ALL-PRO 100, MEDSCOPE, ALL-PRO 2010 and AII-PRO 100 PLUS AND ALL-PRO 200.