Microtech, Inc.
Also registered as Microtech
United StatesFDA applicant, unverified FDA FEI 3004014624
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Microtech Push Button Handpiece, Model Mhs-A100 Ref K022535
Regimes: 510(k) Registry: 510(k)Bartell Small Incision Lens Glide Ref K854994
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3004014624
- Address
- 3030 S. Fairview Street, Suite A, Santa Ana, CA, 92704
Frequently asked questions
How many devices does Microtech, Inc. have in the registry?
The registry currently lists 2 devices for Microtech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microtech, Inc.'s devices?
Among its 2 most recently registered devices, Microtech, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Microtech, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Microtech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Microtech, Inc. in the registry?
The most recently registered devices listed for Microtech, Inc. include MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 and BARTELL SMALL INCISION LENS GLIDE.