Data / Medical devices / United States / Basic Medical Technology Inc.
Basic Medical Technology Inc.: FDA-registered device maker in Ontario, CA, United States, 1 510(k) clearance
Basic Medical Technology Inc. is registered with the FDA (registration 3042372518) in Ontario, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated October 5, 2005. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3042372518
- Address
- 5300 Concours, Ontario, CA, United States, 91764
- Owner or operator
- BASIC MEDICAL TECHNOLOGY INC. (10094275)
- Roles
- Manufacturer
- First device listed
- August 31, 2026
- Registered through
- 2026
- Brand names listed
- MANUAL WHEELCHAIR, REPAIR OR CHANGE PARTS
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Wheelchair, Mechanical | IOR | 1 | 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 |
|---|---|---|---|---|---|---|
| October 5, 2005 | K052468 | YK9000 SERIES MANUAL WHEELCHAIR | IOR | Substantially Equivalent | Intco Metal Products (Zhenjiang) Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 5, 2005. 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.