Progeny, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Progeny, Inc. makes
Progeny, Inc. manufactures intraoral X-ray systems, including the JB-70 model and related configurations, as well as intraoral dental X-ray sensors such as the PROGENY MPSE. The company also produces extraoral imaging equipment like the PREVA system with various arm lengths (76IN, 66IN, 56IN) and associated models, along with imaging software under the PROGENY IMAGING SOFTWARE designation.
The devices in Progeny, Inc.'s portfolio are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Vivid, Models 40-A0001, 40-A0004, 40-A0006 Ref K090079
Regimes: 510(k) Registry: 510(k)Progeny Mpse Intraoral Dental X-Ray Sensor Ref K041831
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 Progeny, Inc. have in the registry?
The registry currently lists 5 devices for Progeny, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Progeny, Inc.'s devices?
Among its 5 most recently registered devices, Progeny, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Progeny, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Progeny, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Progeny, Inc. in the registry?
The most recently registered devices listed for Progeny, Inc. include JB-70 INTRAORAL X-RAY SYSTEM, MODELS 30-A0001/A0002, VIVID, MODELS 40-A0001, 40-A0004, 40-A0006, PROGENY MPSE INTRAORAL DENTAL X-RAY SENSOR and PREVA, 76IN ARM, 66IN ARM, 56IN ARM, MODELS P7017, P7016, P7015.