Data / Medical devices / Canada / Tanses Technologies, Inc.
Tanses Technologies, Inc.: FDA-registered device maker in FABREVILLE Quebec, Canada, 3 510(k) clearances
Tanses Technologies, Inc. is registered with the FDA (registration 8022254) in FABREVILLE Quebec, Canada. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 11, 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
- 8022254
- FEI number
- 3003571423
- Address
- 4450 Hwy. 13, FABREVILLE Quebec, Canada, H7R 6E9
- Owner or operator
- TANSES TECHNOLOGIES, INC. (8022254)
- Roles
- Manufacturer
- First device listed
- January 13, 1997
- Registered through
- 2026
- Brand names listed
- Collagentex RX-1, Collagentex RX-1-Seat, Collagentex RX-2, Collagentex RX-3, Collagentex RX-6, THY-SCANNER, TT-50 series, Tanses and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Booth, Sun Tan | LEJ | 2 | Manufacturer | accessdata.fda.gov |
| Lamp, Infrared, Therapeutic Heating | ILY | 2 | Manufacturer | accessdata.fda.gov |
| Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy | NHN | 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 11, 2018 | K180585 | Collagentex Rx-6 | NHN | Substantially Equivalent | Tanses Technologies, Inc. | accessdata.fda.gov |
| December 22, 2016 | K162022 | Collagentex Rx-1 | NHN | Substantially Equivalent | Tanses Technologies, Inc. | accessdata.fda.gov |
| April 29, 2016 | K152412 | T-32;T-40;T-44;T-52;T-72;TT-50 | LEJ | Substantially Equivalent | Tanses Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Lamp, Infrared, Therapeutic Heating
- All makers of Booth, Sun Tan
- All makers of Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Updated May 11, 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.