FDA.reportPublic FDA data

ACME-MONACO CORP.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
12223011000121071ACME-MONACO CORP.1N2026-01-011450 Central Drive PRESQUE ISLE ME US 04769
12931411293141ACME-MONACO CORP.1N2026-01-0175 Winchell Rd NEW BRITAIN CT US 06052

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
D97277G0U219250Archwire - NITI REVERSE 19X25 U PK108602241349acmecorp@acmemonaco.com
D972AMC1030NTI150Spring - "NiTi open coil spring .010"" x .030"", 15"" (380mm) spool"8602241349acmecorp@acmemonaco.com
D972AMC1616LGRST0Archwire - SS Euro-Form square archwire lower .016" x .016" (Pack of 10 pieces)8602241349acmecorp@acmemonaco.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
308052019834439K920884GUIDEWIRES, VARIOUS TYPESDQX1992-08-19
308062019834439K920884GUIDEWIRES, VARIOUS TYPESDQX1992-08-19
308051562073197K113162SLIDEWIRETM(TRADEMARK PENDING)DQX2012-07-20
308051017369732
308061017369732
308051275077624
308051332608417
308061332608417
308051591834068
308061591834068
308051881881458
308051954316638
308061954316638
308052061737918
308062061737918

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
DQX32012-07-20

PMN#

GUDID#

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