Data / Medical devices / United States / Portable Therapeutix
Portable Therapeutix: FDA-registered device maker in Houston, TX, United States, 2 510(k) clearances
Portable Therapeutix is registered with the FDA (registration 3010201075) in Houston, TX, United States. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated March 11, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010201075
- Address
- 9000 Southwest Fwy Suite 424, Houston, TX, United States, 77074
- Owner or operator
- Portable Therapeutix (10044036)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- April 22, 2013
- Registered through
- 2026
- Brand names listed
- Squid Active Cold Compression, Squid Cold Pack, Squid RX Compression System, Squid Wrap
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Massager, Powered Inflatable Tube | IRP | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Pack, Hot Or Cold, Reusable | IME | 1 | Repackager or relabeler, Specification developer | 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 |
|---|---|---|---|---|---|---|
| March 11, 2014 | K133483 | PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK FOR OTC USE | IRP | Substantially Equivalent | Portable Therapeutix | accessdata.fda.gov |
| April 3, 2013 | K123829 | PORTABLE THERAPEUTIX SQUID ACTIVE COLD COMPRESSION DEVICE AND COLD PACK | IRP | Substantially Equivalent | Portable Therapeutix, LLC | accessdata.fda.gov |
Compare with other makers
Updated March 11, 2014. 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.