Data / Medical devices / Oximeter, Reprocessed / United States
FDA-registered makers of Oximeter, Reprocessed in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Oximeter, Reprocessed (product code NLF). 7 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Oximeter, Reprocessed
- Product code
- NLF
- Country
- United States
Makers of Oximeter, Reprocessed in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Sustainability Solutions | Tempe, AZ, United States | Reprocessor, Specification developer | 6 | October 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| Stryker Sustainability Solutions - Chandler | Chandler, AZ, United States | Reprocessor | 6 | October 22, 2024 | 0 | 0 | 0 | api.fda.gov |
| Renu Medical, Inc. | Everett, WA, United States | Complaint file establishment, Repackager or relabeler, Reprocessor | 4 | November 16, 2011 | 0 | 0 | 0 | api.fda.gov |
| Medline ReNewal | Redmond, OR, United States | Reprocessor | 2 | July 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Lafayette, CO, United States | Specification developer | 1 | December 13, 2004 | 0 | 0 | 0 | api.fda.gov |
| Masimo Corporation | Irvine, CA, United States | Complaint file establishment, Specification developer | 1 | July 28, 2011 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | July 22, 2020 | 0 | 0 | 0 | api.fda.gov |
| Nypro Inc (Maple Grove) | Maple Grove, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.