Data / Medical devices / Taiwan / Blessing Cathay Corporation
Blessing Cathay Corporation: FDA-registered device maker in New Taipei City, Taiwan, 1 510(k) clearance
Blessing Cathay Corporation is registered with the FDA (registration 3033484057) in New Taipei City, Taiwan. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 3, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033484057
- Address
- 2F, No. 310, Jianguo 1st Road, Xinzhuang District, New Taipei City, Taiwan, 242047
- Owner or operator
- Blessing Cathay Corporation (10091747)
- Roles
- Manufacturer
- First device listed
- October 29, 2024
- Registered through
- 2026
- Brand names listed
- AFO Splints, AquaCast Mask, AquaCast Thermoplastics, Cockup Splints, Conformal Bolus, Intrinsic Plus Resting Splints, Oral Bites, Prone Holders and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accelerator, Linear, Medical | IYE | 2 | Manufacturer | accessdata.fda.gov |
| Holder, Head, Radiographic | IWY | 1 | Manufacturer | accessdata.fda.gov |
| Shield, Protective, Personnel | KPY | 1 | Manufacturer | accessdata.fda.gov |
| Splint, Extremity, Non-Inflatable, External, Non-Sterile | NOC | 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 |
|---|---|---|---|---|---|---|
| September 3, 2025 | K252174 | AquaCast Mask | IYE | Substantially Equivalent | Blessing Cathay Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Holder, Head, Radiographic
- All makers of Splint, Extremity, Non-Inflatable, External, Non-Sterile
- All makers of Accelerator, Linear, Medical
- All makers of Shield, Protective, Personnel
Updated September 3, 2025. 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.