Data / Medical devices / United States / Taibo Medical Supply Inc.
Taibo Medical Supply Inc.: FDA-registered device maker in Las Vegas, NV, United States, 1 510(k) clearance
Taibo Medical Supply Inc. is registered with the FDA (registration 3042953785) in Las Vegas, NV, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated June 1, 2015. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3042953785
- Address
- 5595 Spring Mountain Rd Ste B, Las Vegas, NV, United States, 89146
- Owner or operator
- TAIBO Medical Supply Inc. (10094681)
- Roles
- Specification developer
- First device listed
- March 1, 2026
- Registered through
- 2026
- Brand names listed
- Gauze sponge, Medical Tape, Silver Alginate Dressing, Super Absorbent Dressing, Taibo
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Specification developer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Specification developer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 1, 2015 | K143335 | Roosin Silver Calcium Alginate Dressing (Prescription), Roosin Alginate Dressing with Preservative (OTC) | FRO | Substantially Equivalent | Roosin Medical Devices Co., Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Occlusive
- All makers of Dressing, Wound, Drug
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Tape And Bandage, Adhesive
Updated June 1, 2015. 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.