Data / Medical devices / United States / Surgitech, Inc.
Surgitech, Inc.: FDA-registered device maker in Carlsbad, CA, United States, 1 510(k) clearance
Surgitech, Inc. is registered with the FDA (registration 2032724) in Carlsbad, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 14, 2003. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2032724
- FEI number
- 3004014634
- Address
- 2772 Gateway Rd, Carlsbad, CA, United States, 92009
- Owner or operator
- Surgitech, Inc. (10023623)
- Roles
- Specification developer
- First device listed
- December 5, 2007
- Registered through
- 2026
- Brand names listed
- Chronic Pain Suppressor CPS-2000
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Interferential Current Therapy | LIH | 2 | 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 |
|---|---|---|---|---|---|---|
| November 14, 2003 | K033358 | CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000 | LIH | Substantially Equivalent | Surgitech, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 14, 2003. 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.