FDA applicant
Symbiosis Corp.
FDA records 34 decisions for Symbiosis Corp. (Miami, FL) from 1989 to 1996: 34 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and GCJ (Laparoscope, General & Plastic Surgery). 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 Symbiosis Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Symbiosis Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Symbiosis Corp.’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