Micron Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Micron Technology, Inc. makes
Micron Technology, Inc. manufactures the ULTRABLADE, a Class I medical device, and the PEAK OVULATION PREDICTOR, a fertility monitoring tool designed to assist in tracking ovulation cycles.
These devices are regulated under the FDA’s 510(k) pathway as Class I medical devices and are listed in the FDA’s 510(k) database. The company is based in the United States.
Catalogue
Ultrablade Ref K921167
Regimes: 510(k) Registry: 510(k)Peak Ovulation Predictor Ref K863121
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Micron Technology, Inc. have in the registry?
The registry currently lists 2 devices for Micron Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micron Technology, Inc.'s devices?
Among its 2 most recently registered devices, Micron Technology, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Micron Technology, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Micron Technology, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Micron Technology, Inc. in the registry?
The most recently registered devices listed for Micron Technology, Inc. include ULTRABLADE and PEAK OVULATION PREDICTOR.