FDA.reportPublic FDA data

Artelon

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30332735263033273526Artelon1N2026-01-01380 Michel St. N.W Suite A ATL GA US 30313

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
00850003396163FlexBand - MULTI KIT(800) 610-3446tiffini.wittwer@artelon.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3327811049784949K230316FlexBand; FlexPatch; FlexBand PlusOWW2023-05-26
3327812062712414K200503ATL AnchorsMBI2020-09-02
3327811503847797

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OWW12023-05-26
MBI12020-09-02

GUDID#

41 records. Showing 1-40. Next