FDA applicant
Fertility Technology Resources, Inc.
FDA records 4 decisions for Fertility Technology Resources, Inc. (Marietta, GA) from 1999 to 2004: 4 510(k) clearances. Most are in product codes MQF (Catheter, Assisted Reproduction) and MQE (Needle, Assisted Reproduction). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Fertility Technology Resources, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Fertility Technology Resources, Inc. since 2007.
Recalls per year
2in 2007
Class I Class II/III not classified
Planning a device like Fertility Technology Resources, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Fertility”
FDA records each applicant name separately; these may or may not be the same firm.