Data / Medical devices / United States / Taylor Healthcare Products, Inc
Taylor Healthcare Products, Inc: FDA-registered device maker in Spring, TX, United States, 1 510(k) clearance
Taylor Healthcare Products, Inc is registered with the FDA (registration 3009149661) in Spring, TX, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated September 3, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009149661
- Address
- 605 Spring Hill Drive, Spring, TX, United States, 77386
- Owner or operator
- Taylor Healthcare Products, Inc (10056341)
- Roles
- Specification developer
- First device listed
- November 30, 2017
- Registered through
- 2026
- Brand names listed
- Taylor Healthcare Products, Inc.
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bedding, Disposable, Medical | KME | 1 | Specification developer | accessdata.fda.gov |
| Container, Sharps | MMK | 2 | Specification developer | accessdata.fda.gov |
| Cover, Mattress (Medical Purposes) | FMW | 1 | Specification developer | accessdata.fda.gov |
| Stretcher, Hand-Carried | FPP | 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 |
|---|---|---|---|---|---|---|
| September 3, 2008 | K082042 | GONGDONG DISPOSABLE SHARP CONTAINER | MMK | Substantially Equivalent | Zhejiang Gongdong Medical Plastic Factory | accessdata.fda.gov |
Compare with other makers
- All makers of Bedding, Disposable, Medical
- All makers of Stretcher, Hand-Carried
- All makers of Container, Sharps
- All makers of Cover, Mattress (Medical Purposes)
Updated September 3, 2008. 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.