FDA.reportPublic FDA data

Embolization Inc

Matched from indexed company URL: Embolization, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30429531523042953152Embolization Inc1N2026-01-015421 Western Ave Boulder CO US 80301

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
10857798005093Nitinol Enhanced Device - Peripheral vascular embolization device Framing 3-4mm Vessel Diameter303-531-1238inquire@embolizationinc.com
10857798005109Nitinol Enhanced Device - Peripheral vascular embolization device Framing 4-5mm Vessel Diameter303-531-1238inquire@embolizationinc.com
10857798005123Nitinol Enhanced Device - Peripheral vascular embolization device Packing 3-5mm Vessel Diameter303-531-1238inquire@embolizationinc.com
10857798005130Nitinol Enhanced Device - Peripheral vascular embolization device Framing 2-3mm Vessel Diameter303-531-1238inquire@embolizationinc.com
10857798005147Nitinol Enhanced Device - Peripheral vascular embolization device Packing 2-3mm Vessel Diameter303-531-1238inquire@embolizationinc.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3460891540081242K250276Nitinol Enhanced Device (NED)KRD2025-05-15

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KRD12025-05-15

GUDID#