FDA.reportPublic FDA data

STINGRAY SURGICAL PRODUCTS

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30060599173006059917STINGRAY SURGICAL PRODUCTS1N2026-01-011701 Costa Del Sol Boca Raton FL US 33432

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
988211562551650K972901AMERICAN BIOSURGICAL ELECTROSURGICAL BIPOLAR CABLE/CORDGEI1997-09-19
988211624365347K971540AMERICAN BIOSURGICAL ELECTROSURGICAL MONOPOLAR CABLE/CORDGEI1997-08-14
988211855518685K953889AMERICAN BIOSURGICAL ELECTROSURGICAL BIPOLAR CABLE/CORDGEI1995-10-18
988211680781925K123478STINGRAY BIPOLAR FORCEPSGEI2013-05-10
988211205961985K102752STINGRAY ULTRALITE DISPOSABLE IRRIGATING BIPOLAR FORCEPSGEI2011-11-09
988211713690318K042608TECNO REUSABLE BIPOLAR CABLES, MODEL 190-100 AND 190-110GEI2004-10-18
988211187497210
988211553262061
988211641031176
988211686098474

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
GEI62013-05-10

PMN#