Data / Medical devices / Single-Use Reprocessed Ultrasonic Surgical Instruments
Single-Use Reprocessed Ultrasonic Surgical Instruments (NLQ): 7 FDA-registered makers in 2 countries
7 establishments in 2 countries are registered with the FDA to make Single-Use Reprocessed Ultrasonic Surgical Instruments (product code NLQ, Class U). 6 of them have a 510(k) clearance or PMA approval on file and 3 have a recall event. The FDA has issued 27 510(k) clearances under this code, the latest on August 14, 2025, and lists 7 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- NLQ
- Device class
- U
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| United States | 6 |
| Mexico | 1 |
Makers of Single-Use Reprocessed Ultrasonic Surgical Instruments
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Stryker Sustainability Solutions Lakeland | Lakeland, FL, United States | Reprocessor | 12 | August 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Stryker Sustainability Solutions | Tempe, AZ, United States | Reprocessor, Specification developer | 7 | August 14, 2025 | 0 | 3 | 0 | api.fda.gov |
| Stryker Sustainability Solutions - Chandler | Chandler, AZ, United States | Reprocessor | 7 | August 14, 2025 | 0 | 0 | 0 | api.fda.gov |
| Medline ReNewal | Redmond, OR, United States | Reprocessor | 5 | August 19, 2020 | 0 | 1 | 0 | api.fda.gov |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 1 | August 19, 2020 | 0 | 2 | 0 | api.fda.gov |
| Stryker Tijuana Operations | Tijuana Baja California, Mexico | Reprocessor | 1 | April 5, 2017 | 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 August 14, 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.