FDA.reportPublic FDA data

Altivera Medical, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
17236863000214920Altivera Medical, Inc.1N2026-01-018181 E Tufts Ave Ste 200 Denver CO US 80237
30179369743017936974Altivera Medical, Inc.1N2026-01-0114800 Grasslands Drive Englewood CO US 80112

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
529841777989334K991241IF8000IPF1999-11-02
529841312182412K914925MEDAC SYSTEM/3HCC1993-10-21
529841908309423K914920BIOFEEDBACK SYSTEM/3HCC1992-11-16
529841991787748K241228TENSWaveGZJ2024-08-27
2870381991787748K241228TENSWaveGZJ2024-08-27
2870381765632907K233485M-WaveIPF2024-01-26
2870381402548086K222669Cryopush Cold Compression DeviceIRP2022-12-05
529842049338768K121820INWAVEKPI2012-08-24
2870382049338768K121820INWAVEKPI2012-08-24
529841586692400K111279NEXWAVE COMBO MUSCLE STIMULATOR SYSTEMIPF2011-09-20
2870381586692400K111279NEXWAVE COMBO MUSCLE STIMULATOR SYSTEMIPF2011-09-20
529841870996629K013210TRUWAVEGZJ2002-04-04
529841985617405K012885NEUROMOVE NM900IPF2001-11-08
2870381985617405K012885NEUROMOVE NM900IPF2001-11-08
529841291109186K010745EMS 3000IPF2001-06-27

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
IPF72024-01-26
GZJ32024-08-27
KPI22012-08-24
HCC21993-10-21
IRP12022-12-05