ClearanceBrief
510(k) K172390 ยท HCG Device, Neurovascular Embolization

Optima Coil System

ApplicantBlockade Medical, LLC (D.B.A. Balt Usa), Irvine CA, US
DecisionSubstantially Equivalent, Feb 18, 2018
ReceivedAug 8, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172390

DateFirm and productCodeLinked 510(k)
Jun 18, 2025BALT USA, LLC
Optima Coil System REFs/UDI-DI codes: OPTI0156BLK 00810068568875 OPTI0158BLK 00810068568882 OPTI0103BLK 00810068568851 OPTI0258BLK 00810068568929 OPTI0212BLK 00810068568912 OPTI0206BLK 00810068568905
Open, Classified
HCGNone listed
Feb 8, 2024BALT USA, LLC
Neurovascular embolization device. The Optima Coil System is a series specialized coils that are inserted into the vasculature under angiographic visualization to embolize intracranial aneurysms and o
Open, Classified
HCGNone listed
Oct 20, 2022BALT USA, LLC
Optima Coil System Model Number OPTI0208CSS10, Model Number OPTI0308CSS10. Used in endovascular procedures.
Open, Classified
HCGNone listed
Jul 26, 2022BALT USA, LLC
Optima Coil System Model OPTI0520CSF10. For endovascular embolization.
Open, Classified
HCGNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.