Data / Medical devices / Taiwan / Genemax Medical Products Industry Corp.
Genemax Medical Products Industry Corp.: FDA-registered device maker in Taichung City, Taiwan, 2 510(k) clearances
Genemax Medical Products Industry Corp. is registered with the FDA (registration 3003123807) in Taichung City, Taiwan. It lists 10 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 12, 2004. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003123807
- Address
- No. 86, Lane 226 Tai-Ming Road, Wu-Jih District, Taichung City, Taiwan, 41468
- Owner or operator
- GENEMAX MEDICAL PRODUCTS INDUSTRY CORP. (9056696)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- June 18, 2004
- Registered through
- 2026
- Brand names listed
- Exer-Rest, GENEMAX, GENEMAX Commode, GENEMAX Infusion Stand, Medline Excel Wheelchair, Non-Measuring Exerciser, Rollator & Accessories, Therapeutic Vibrator and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Adaptor, Hygiene | ILS | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Exerciser, Non-Measuring | ION | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Vibrator, Therapeutic | IRO | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Walker, Mechanical | ITJ | 1 | Exporter to the US, Manufacturer | accessdata.fda.gov |
| Wheelchair, Mechanical | IOR | 1 | Contract manufacturer | accessdata.fda.gov |
| Wheelchair, Powered | ITI | 2 | Exporter to the US, 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 |
|---|---|---|---|---|---|---|
| November 12, 2004 | K042749 | GENEMAX POWER WHEELCHAIR, PW4 | ITI | Substantially Equivalent | Genemax Medical Products Industry Corp. | accessdata.fda.gov |
| November 12, 2004 | K042748 | GENEMAX POWER WHEELCHAIR, PW3 | ITI | Substantially Equivalent | Genemax Medical Products Industry Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Exerciser, Non-Measuring
- All makers of Wheelchair, Mechanical
- All makers of Bed, Ac-Powered Adjustable Hospital
- All makers of Walker, Mechanical
- All makers of Components, Wheelchair
- All makers of Bed, Manual
Updated November 12, 2004. 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.