Angstrom Mfg., Inc.
United StatesFDA applicant, unverified FDA FEI 3003610374
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Disposable Prophy Angle Ref K103157
Regimes: 510(k) Registry: 510(k)Straight Handpiece Adapter; Contra Handpiece Adapter; Twist Handpiece Adapter; Flex Handpiece Adapter Ref K103158
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3003610374
- Address
- 4 Trautman Industrial Court, Sainte Genevieve, MO, 63670
Frequently asked questions
How many devices does Angstrom Mfg., Inc. have in the registry?
The registry currently lists 2 devices for Angstrom Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angstrom Mfg., Inc.'s devices?
Among its 2 most recently registered devices, Angstrom Mfg., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Angstrom Mfg., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angstrom Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Angstrom Mfg., Inc. in the registry?
The most recently registered devices listed for Angstrom Mfg., Inc. include DISPOSABLE PROPHY ANGLE and STRAIGHT HANDPIECE ADAPTER; CONTRA HANDPIECE ADAPTER; TWIST HANDPIECE ADAPTER; FLEX HANDPIECE ADAPTER.