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ARCERA GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30153738203015373820ARCERA GMBH1N2026-01-01Levelingstrasse 8 Munich Bavaria DE 81673

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2291141223394823P980044SUPARTZ FXMOZ2001-01-24
2291141641965309P940015SYNVISC ONEMOZ1997-08-08
2291141221881020P170007DUROLANEMOZ2017-08-29
2291141830555503P140029Restylane Refyne, Restylane DefyneLMH2016-12-09
2291141770086243P110033JUVEDERM VOLUMA XCLMH2013-10-22
2291141430060533P090031MONOVISCMOZ2014-02-25
2291141734684567P090016BELOTERO BALANCELMH2011-11-14
2291141250337702P050052RADIESSE INJECTABLE IMPLANTLMH2006-12-22
2291141449259780P050047JUVEDERM 24HV, JUVEDERM 30 AND JUVEDERM 30HV GEL IMPLANTSLMH2006-06-02
2291141935198316P050037RADIESSE 1.3CC AND 0.3CCLMH2006-12-22
2291141342099307P040024RESTYLANE INJECTABLE GELLMH2005-03-25
2291141620786834P030050SCULPTRA AND SCULPTRA AESTHETICLMH2004-08-03
2291141941949070P030019ORTHOVISC HIGH MOLECULAR WEIGHT HYALURONANMOZ2004-02-04
2291141290539006P010029EUFLEXXA (1% SODIUM HYALURONATE)MOZ2004-12-03

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
LMH142016-12-09
MOZ112017-08-29

GUDID#