FDA.reportPublic FDA data

Silq Technologies Corporation

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30146500733014650073Silq Technologies Corporation1N2026-01-01323 Sunny Isles Blvd. 7th Floor Sunny Isles Beach FL US 33160

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
00850041415178ClearTract - 2-Way 100% Silicone, 20Fr X 10ml, ClearTract SPT Catheter9497352614Ethanr@silq.tech
00850041415185ClearTract - 2-Way 100% Silicone, 22Fr X 10ml, ClearTract SPT Catheter9497352614ethanr@silq.tech

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2800731939959332K192034HDX 100% Silicone 2-way Foley Catheter, 14Fr/10cc, HDX 100% Silicone 2-way Foley Catheter, 16Fr/5cc, HDX 100% Silicone 2-way Foley Catheter, 18Fr/10ccEZL2020-04-21

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
EZL12020-04-21

PMN#

GUDID#