FDA applicant
Gsi Development Co.
FDA records 4 decisions for Gsi Development Co. (Carmel, NY) from 1988 to 1993: 4 510(k) clearances. Most are in product codes IOQ (Bed, Flotation Therapy, Powered) and INX (Bed, Air Fluidized). 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 Gsi Development Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Gsi Development Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Gsi Development Co.’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