Bioptics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Bioptics, Inc. makes
Bioptics, Inc. makes digital specimen radiography systems, including the BioVision Digital Specimen Radiography System, PixArray 100 Digital Specimen Radiography (DSR) System, and Core Vision Digital Specimen Radiography (DSR) System.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
10 X 10 Vision Ref K091928
Regimes: 510(k) Registry: 510(k)Biovision Digital Specimen Radiography System Ref K091558
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioptics, Inc. have in the registry?
The registry currently lists 4 devices for Bioptics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioptics, Inc.'s devices?
Among its 4 most recently registered devices, Bioptics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Bioptics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Bioptics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioptics, Inc. in the registry?
The most recently registered devices listed for Bioptics, Inc. include 10 X 10 VISION, BIOVISION DIGITAL SPECIMEN RADIOGRAPHY SYSTEM, PIXARRAY 100 DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM and CORE VISION DIGITAL SPECIMEN RADIOGRAPHY (DSR) SYSTEM.