FDA.reportPublic FDA data

GUIDESTAR MEDICAL DEVICES INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30299602853029960285GUIDESTAR MEDICAL DEVICES INC.1N2026-01-01201-2067 Cadboro Bay Rd Victoria British Columbia CA V8R5G4

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
00860011139607EpiZact - EpiZact is a single use medical device used during an epidural procedure.1-250-686-7832ryan@guidestarmd.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3221951522624467K233056EpiZactFMF2023-11-02

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
FMF12023-11-02

PMN#

EpiZact

2023-11-02

Guidestar Medical Devices

GUDID#