PROSIDYAN, INC.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30110150973011015097PROSIDYAN, INC.1N2026-01-0141 Spring Street #107 New Providence NJ US 07974

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
1724271266617112K251648GPS Advanced; GPS Advanced CannulaFMF2025-06-24
1724272016873049K213803FIBERGRAFT Aeridyan Matrix Bone Graft SubstituteMQV2022-08-23
1724271694971738K180080FIBERGRAFT BG Matrix Bone Graft SubstituteMQV2018-04-06
1724271696955784K171284FIBERGRAFT BG Matrix Bone Graft SubstituteMQV2017-06-30
1724271014714606K170306FIBERGRAFT BG Putty Bone Graft SubstituteMQV2017-05-24
1724271853402230K151154FIBERGRAFT BG MorselsMQV2015-11-10
1724272051398276K143533FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTEMQV2015-03-25
1724271078257034K141956FIBERGRAFT BG MORSELSMQV2014-08-13
1724271779919475K132805BG MORSELSMQV2014-03-14

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQV82022-08-23
FMF12025-06-24

PMN#