Data / Medical devices / Taiwan / Microp Technology (taiwan), Inc.
Microp Technology (taiwan), Inc.: FDA-registered device maker in Chiayi City Chiayi(County), Taiwan, 1 510(k) clearance
Microp Technology (taiwan), Inc. is registered with the FDA (registration 3013287728) in Chiayi City Chiayi(County), Taiwan. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 24, 2018. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013287728
- Address
- No. 50, Zhongxiao 2nd St., East Dist., Chiayi City Chiayi(County), Taiwan, 600
- Owner or operator
- MicroP Technology (Taiwan), Inc. (10058189)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- July 31, 2018
- Registered through
- 2026
- Brand names listed
- Dental Handpieces and Accessories HALLEY Series, Dental High-speed Handpiece HALLEY Series
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Handpiece, Air-Powered, Dental | EFB | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Handpiece, Contra- And Right-Angle Attachment, Dental | EGS | 1 | Contract manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 24, 2018 | K173943 | Dental High-speed Handpiece and Accessories | EFB | Substantially Equivalent | Microp Technology (Taiwan), Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Handpiece, Air-Powered, Dental
- All makers of Handpiece, Contra- And Right-Angle Attachment, Dental
Updated July 24, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.