Data / Medical devices / United States / Strategic Lab Partners LLC
Strategic Lab Partners LLC: FDA-registered device maker in Memphis, TN, United States, 1 510(k) clearance
Strategic Lab Partners LLC is registered with the FDA (registration 3017014794) in Memphis, TN, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 19, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017014794
- Address
- 5875 E Shelby Dr, Memphis, TN, United States, 38141
- Owner or operator
- STRATEGIC LAB PARTNERS LLC (10075297)
- Roles
- Repackager or relabeler, Reprocessor
- First device listed
- June 11, 2020
- Registered through
- 2026
- Brand names listed
- Primestore MTM
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Microbial Nucleic Acid Storage And Stabilization Device | QBD | 2 | Repackager or relabeler, Reprocessor | 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 |
|---|---|---|---|---|---|---|
| March 19, 2018 | DEN170029 | PrimeStore MTM | QBD | Unknown | Longhorn Vaccines and Diagnostics, LLC | accessdata.fda.gov |
Compare with other makers
Updated March 19, 2018. 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.