Data / Medical devices / United States / Import Warehouse Inc
Import Warehouse Inc: FDA-registered device maker in Dallas, TX, United States, 1 510(k) clearance
Import Warehouse Inc is registered with the FDA (registration 3003370588) in Dallas, TX, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 12, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003370588
- Address
- 11029 Harry Hines Blvd Ste A, Dallas, TX, United States, 75229
- Owner or operator
- Import Warehouse Inc (10094963)
- Roles
- Repackager or relabeler
- First device listed
- January 10, 2026
- Registered through
- 2026
- Brand names listed
- TROJAN
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Condom | HIS | 2 | Repackager or relabeler | 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 12, 2010 | K092586 | MALE LATEX CONDOM (STRAIGHT SIDE OR CONTOURED OR FLARED IN SHAPE, EITHER TEXTURED OR NON-TEXTURED , LUBRICATED OR NON-LU | HIS | Substantially Equivalent | Innolatex (Thailand) Limited | accessdata.fda.gov |
Compare with other makers
Updated May 12, 2010. 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.