FDA applicant
Endotherapeutics
FDA records 7 decisions for Endotherapeutics (Redwood City, CA) from 1984 to 1987: 7 510(k) clearances. Most are in product codes HET (Laparoscope, Gynecologic (And Accessories)) and FHO (Pneumoperitoneum Needle). 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 Endotherapeutics’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Endotherapeutics since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Endotherapeutics’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) Report