Data / Medical devices / Laparoscope, General & Plastic Surgery, Reprocessed / United States
FDA-registered makers of Laparoscope, General & Plastic Surgery, Reprocessed in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Laparoscope, General & Plastic Surgery, Reprocessed (product code NLM). 6 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.
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- Device
- Laparoscope, General & Plastic Surgery, Reprocessed
- Product code
- NLM
- Country
- United States
Makers of Laparoscope, General & Plastic Surgery, Reprocessed in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Sustainability Solutions Lakeland | Lakeland, FL, United States | Reprocessor | 10 | July 31, 2020 | 0 | 3 | 0 | api.fda.gov |
| Medline ReNewal | Redmond, OR, United States | Reprocessor | 4 | April 15, 2019 | 0 | 1 | 0 | api.fda.gov |
| Stryker Sustainability Solutions | Tempe, AZ, United States | Reprocessor, Specification developer | 3 | July 31, 2020 | 0 | 5 | 0 | api.fda.gov |
| Stryker Sustainability Solutions - Chandler | Chandler, AZ, United States | Reprocessor | 3 | July 31, 2020 | 0 | 0 | 0 | api.fda.gov |
| Renovo, Inc. | Bend, OR, United States | Reprocessor | 2 | October 6, 2017 | 0 | 0 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | April 15, 2019 | 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.