Data / Medical devices / Taiwan / Caremed Supply, Inc.
Caremed Supply, Inc.: FDA-registered device maker in New Taipei City, Taiwan, 2 510(k) clearances
Caremed Supply, Inc. is registered with the FDA (registration 8022590) in New Taipei City, Taiwan. It lists 6 device types. The FDA files 2 510(k) clearances under its listings, the newest dated December 4, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 8022590
- FEI number
- 3495
- Address
- 7F., No.2, Lane 235, Bao Chiao RD. Xin Tien Dist., New Taipei City, Taiwan, 23145
- Owner or operator
- Caremed Supply, Inc. (9102439)
- Roles
- Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer
- First device listed
- September 22, 2009
- Registered through
- 2026
- Brand names listed
- AIR-MATT TRANSFER MAT, Ai1 Premium, AllCare ACGOVDynamic Mattress Pump, B-Safe, COMFORT GLIDE AIR BLOWER, Century Gold, Comfort Glide, ComfortTemp and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bed, Ac-Powered Adjustable Hospital | FNL | 2 | Contract manufacturer, Exporter to the US, Foreign private label distributor, Manufacturer | accessdata.fda.gov |
| Device, Transfer, Patient, Manual | FMR | 1 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mattress, Air Flotation, Alternating Pressure | FNM | 2 | Contract manufacturer, Exporter to the US, Manufacturer | accessdata.fda.gov |
| Mattress, Flotation Therapy, Non-Powered | IKY | 1 | Manufacturer | accessdata.fda.gov |
| Sleeve, Limb, Compressible | JOW | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| System, Thermal Regulating | DWJ | 2 | Contract 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 |
|---|---|---|---|---|---|---|
| December 4, 2014 | K141064 | VESOFLOW PLUS DVT COMPRESSION DEVICE | JOW | Substantially Equivalent | Caremed Supply, Inc. | accessdata.fda.gov |
| August 25, 2011 | K110977 | VESOFLOW | JOW | Substantially Equivalent | Caremed Supply, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Sleeve, Limb, Compressible
- All makers of System, Thermal Regulating
- All makers of Bed, Ac-Powered Adjustable Hospital
- All makers of Mattress, Flotation Therapy, Non-Powered
- All makers of Device, Transfer, Patient, Manual
- All makers of Mattress, Air Flotation, Alternating Pressure
Updated December 4, 2014. 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.