Data / Medical devices / United States / Nelson Environmental Technologies, Inc.
Nelson Environmental Technologies, Inc.: FDA-registered device maker in Stafford, TX, United States, 3 510(k) clearances
Nelson Environmental Technologies, Inc. is registered with the FDA (registration 3010866895) in Stafford, TX, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated April 11, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010866895
- Address
- 10518 Cash Rd., Stafford, TX, United States, 77477
- Owner or operator
- NELSON ENVIRONMENTAL TECHNOLOGIES, INC. (9039629)
- Roles
- Manufacturer
- First device listed
- December 14, 2007
- Registered through
- 2026
- Brand names listed
- Chlorine Sentinel II (CS-II), Nelson Sentinel Series Basic Chlorine Sentinel, Nelson Water Systems for Hemodialys
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Strip, Test, Reagent, Residuals For Dialysate, Disinfectant | MSY | 2 | Manufacturer | accessdata.fda.gov |
| Subsystem, Water Purification | FIP | 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 |
|---|---|---|---|---|---|---|
| April 11, 2025 | K243898 | Chlorine Sentinel II | MSY | Substantially Equivalent | Nelson Environmental Technologies, Inc. | accessdata.fda.gov |
| October 29, 2020 | K193169 | Nelson Sentinel Series Basic Chlorine Sentinel | MSY | Substantially Equivalent | Nelson Environmental Technologies, Inc. | accessdata.fda.gov |
| May 25, 2000 | K993877 | NELSON WATER SYSTEMS FOR HEMODIALYSIS | FIP | Substantially Equivalent | Nelson Environmental Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Subsystem, Water Purification
- All makers of Strip, Test, Reagent, Residuals For Dialysate, Disinfectant
Updated April 11, 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.