FDA applicant
Endocrine Associates, Inc.
FDA records 2 decisions for Endocrine Associates, Inc. (Houston, TX) in 1987: 2 510(k) clearances. Most are in product codes JKR (Radioimmunoassay, Calcitonin) and JKC (Radioimmunoassay, Dehydroepiandrosterone (Free…). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Endocrine Associates, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Endocrine Associates, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Endocrine Associates, 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 “Endocrine”
FDA records each applicant name separately; these may or may not be the same firm.