Micron Corp.
JapanFDA applicant, unverified FDA FEI 3002820248
Micron Corp. is a medical device manufacturer, with 34 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.
- Devices
- 34
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 29
- FDA 510(k) 5
- Device classes
- FDA Class II 20
- FDA Class I 14
- Identifiers
- FDA FEI 3002820248
At a glance
Market reach
- United States
- FDA FEI
What Micron Corp. makes
Micron Corp. makes pneumatic dental scaling and debridement systems, including handpieces and reusable tips for endodontic use, as well as dental abrasive air jet system handpieces and dental delivery system irrigation handpieces.
Catalogue
Search and filter all 34 devicesCompany details
- FDA FEI number
- 3002820248
- Address
- 2-17-7 Ikgami, OTA-KU Tokyo
Frequently asked questions
How many devices does Micron Corp. have in the registry?
The registry currently lists 34 devices for Micron Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Micron Corp.'s devices?
Among its 34 most recently registered devices, Micron Corp. has devices listed in FDA 510(k) (5 devices) and FDA GUDID (29 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Micron Corp.'s devices fall under?
Among its 34 most recently registered devices, the classes recorded for Micron Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Micron Corp. in the registry?
The most recently registered devices listed for Micron Corp. include The BLASTER BC-B5010, SS17K-B, The BLASTER BC-B5000 and AW-100-4H.