Data / Medical devices / Accessory, Assisted Reproduction / United States
FDA-registered makers of Accessory, Assisted Reproduction in the United States: 7 establishments
7 establishments in the United States are registered with the FDA to make Accessory, Assisted Reproduction (product code MQG). 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
- Accessory, Assisted Reproduction
- Product code
- MQG
- Country
- United States
Makers of Accessory, Assisted Reproduction 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, Repackager or relabeler, Specification developer | 5 | August 19, 2026 | 0 | 2 | 0 | api.fda.gov |
| Thermo Fisher Scientific (asheville) LLC | Marietta, OH, United States | Complaint file establishment, Manufacturer | 3 | May 15, 2002 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Bloomington, IN, United States | Complaint file establishment, Manufacturer | 2 | October 27, 1999 | 0 | 2 | 0 | api.fda.gov |
| Cook Incorporated | Spencer, IN, United States | Manufacturer | 2 | February 1, 1999 | 0 | 0 | 0 | api.fda.gov |
| Cook Incorporated | Ellettsville, IN, United States | Complaint file establishment, Manufacturer | 1 | February 1, 1999 | 0 | 0 | 0 | api.fda.gov |
| LifeGlobal Group, LLC | Trumbull, CT, United States | Specification developer | 1 | September 15, 2000 | 0 | 0 | 0 | api.fda.gov |
| Advanced Instrumentations, Inc. | Miami, FL, United States | Specification developer | 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.