Data / Medical devices / United States / Matia Robotics (us), Inc.
Matia Robotics (us), Inc.: FDA-registered device maker in Salt Lake City, UT, United States, 2 510(k) clearances
Matia Robotics (us), Inc. is registered with the FDA (registration 3014250398) in Salt Lake City, UT, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated May 29, 2020. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3014250398
- Address
- 1929 S 4130 W Unit A, Salt Lake City, UT, United States, 84104
- Owner or operator
- Matia Robotics (US), Inc. (10056899)
- Roles
- Manufacturer
- First device listed
- January 29, 2018
- Registered through
- 2027
- Brand names listed
- TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08, Tek RMD
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Standup | IPL | 2 | 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 |
|---|---|---|---|---|---|---|
| May 29, 2020 | K191334 | Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08 | IPL | Substantially Equivalent | Matia Robotics (Us), Inc. | accessdata.fda.gov |
| June 11, 2015 | K150548 | Tek RMD (Tek Robotic Mobilization Device) | IPL | Substantially Equivalent | Matia Robotics Mekatroik Sis. Ar-Ge Muh. Yaz.San VE Tic.A.S | accessdata.fda.gov |
Compare with other makers
Updated May 29, 2020. 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.