Data / Medical devices / Media, Reproductive / United States
FDA-registered makers of Media, Reproductive in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Media, Reproductive (product code MQL). 6 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Media, Reproductive
- Product code
- MQL
- Country
- United States
Makers of Media, Reproductive in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Coopersurgical, Inc. | Trumbull, CT, United States | Complaint file establishment, Manufacturer, Specification developer | 55 | July 17, 2020 | 0 | 7 | 0 | api.fda.gov |
| Irvine Scientific LLC | Santa Ana, CA, United States | Complaint file establishment, Specification developer | 19 | September 12, 2025 | 0 | 0 | 0 | api.fda.gov |
| LifeGlobal Group, LLC | Trumbull, CT, United States | Specification developer | 12 | February 17, 2015 | 0 | 0 | 0 | api.fda.gov |
| Invitrocare Inc | Frederick, MD, United States | Manufacturer, Repackager or relabeler | 11 | March 23, 2006 | 0 | 0 | 0 | api.fda.gov |
| Vitrolife Inc. | San Diego, CA, United States | Manufacturer | 5 | March 20, 2003 | 0 | 0 | 0 | api.fda.gov |
| Reprolife America, LLC | Kingwood, TX, United States | Manufacturer | 1 | August 27, 2024 | 0 | 0 | 0 | api.fda.gov |
| FUJIFILM Biosciences INC. | Santa Ana, CA, United States | Contract manufacturer | 0 | 0 | 3 | 0 | api.fda.gov | |
| Vitrolife Inc. | Englewood, CO, United States | Contract manufacturer, Manufacturer for export | 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.