Data / Medical devices / Taiwan / Caremed Supply, Inc.
Caremed Supply, Inc.: FDA-registered device maker in Yilan County, Taiwan, 3 510(k) clearances
Caremed Supply, Inc. is registered with the FDA (registration 3013528589) in Yilan County, Taiwan. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 5, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013528589
- Address
- No. 50, Ln. 30, Sanjie 2nd Rd., Wujie Township, Yilan County, Taiwan, 268
- Owner or operator
- Caremed Supply, Inc. (9102439)
- Roles
- Contract manufacturer, Exporter to the US, Manufacturer
- First device listed
- September 14, 2011
- Registered through
- 2026
- Brand names listed
- AIR-MATT TRANSFER MAT, AllCare ACGOVDynamic Mattress Pump, B-Safe, COMFORT GLIDE AIR BLOWER, Century Gold, Comfort Glide, DUET, DYNAFLOW and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| 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 | 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 |
|---|---|---|---|---|---|---|
| August 5, 2018 | K181217 | VesoFlow Lite DVT Compression Device | JOW | Substantially Equivalent | Caremed Supply, Inc. | accessdata.fda.gov |
| 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 Mattress, Flotation Therapy, Non-Powered
- All makers of Mattress, Air Flotation, Alternating Pressure
- All makers of Device, Transfer, Patient, Manual
Updated August 5, 2018. 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.