Data / Medical devices / United States / CT Intl.
CT Intl.: FDA-registered device maker in San Luis Obispo, CA, United States, 5 510(k) clearances
CT Intl. is registered with the FDA (registration 2026990) in San Luis Obispo, CA, United States. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated August 5, 1999. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2026990
- Address
- 4349 Old Santa Fe Rd, San Luis Obispo, CA, United States, 93401
- Owner or operator
- CT INTL. (2026990)
- Roles
- Specification developer
- First device listed
- June 15, 2006
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Polymer Patient Examination Glove | LZA | 1 | Specification developer | accessdata.fda.gov |
| Surgeon'S Gloves | KGO | 1 | 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 |
|---|---|---|---|---|---|---|
| August 5, 1999 | K992019 | LAGLOVE POWDER FREE LATEX SURGICAL GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS OR LESS) | KGO | Substantially Equivalent | La Glove (M) Sdn. Bhd. | accessdata.fda.gov |
| July 12, 1999 | K984512 | NITRILON CORRECT-TOUCH | KGO | Substantially Equivalent | Ct Intl. | accessdata.fda.gov |
| June 22, 1998 | K981333 | NITRILON CORRECT-TOUCH | LZA | Substantially Equivalent | Biopro (M) Sdn Bhd | accessdata.fda.gov |
| June 22, 1998 | K981304 | NITRILON CORRECT-TOUCH | LZA | Substantially Equivalent | Ct Intl. | accessdata.fda.gov |
| September 6, 1989 | K891622 | STERILE SURGICAL NATURAL LATEX GLOVES | KGO | Substantially Equivalent | Ct Intl. | accessdata.fda.gov |
Compare with other makers
Updated August 5, 1999. 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.