FDA.reportPublic FDA data

RAPID MEDICAL INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30155317233015531723RAPID MEDICAL INC.1Y2026-01-01445 South Kimball Avenue Suite 140 Southlake TX US 76092

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2310751380267778K260617Tigertriever 13 Ultra Revascularization DeviceNRY2026-08-28
2310751721002591K254006Drivewire 35 GuidewireMOF2026-07-17
2310752007949785K253146Hyperdrive 35 GuidewireDQX2026-09-18
2310751052487798K253062Tigertriever 25 Revascularization DeviceNRY2026-03-12
2310751979512278K251603Tigertriever 17 Ultra Revascularization DeviceNRY2025-10-06
2310751731675735K233791Drivewire 24 GuidewireMOF2024-07-11
2310751835152560K230429Tigertriever 21 Revascularization Device, Tigertriever 17 Revascularization Device, Tigertriever 13 Revascularization DeviceNRY2023-04-17
2310751967777630K220808Tigertriever 13 Revascularization DeviceNRY2022-07-25
2310751296681072K203625Numen Coil Embolization System; NumenFR Detachment SystemHCG2021-09-01
2310751178430474K203592Tigertriever and Tigertriever 17 Revascularization DevceNRY2021-03-23
2310751939797002K200374Columbus GuidewireMOF2020-12-14
2310751582145977DEN230064BraidE Embolization Assist DeviceQZU2024-02-21
2310751897862302DEN170064Comaneci, Comaneci Petit, Comaneci 17PUU2019-04-24

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
NRY62026-08-28
MOF32026-07-17
DQX12026-09-18
QZU12024-02-21
HCG12021-09-01
PUU12019-04-24