Reprise Biomedical, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30108943433010894343Reprise Biomedical, Inc.1N2026-01-0117400 Medina Road Suite 100 Plymouth MN US 55447
30108943433010894343Reprise Biomedical, Inc.1N2020-04-2517400 Medina Road Suite 100 Plymouth MN US 55447

GUDID Contact Samples#

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2820791937723082K240753Miro3D Fibers Wound MatrixKGN2024-04-19
2820791342241642K240277MiroDry Wound MatrixKGN2024-03-01
2820791158360247K231614MiroTract Wound MatrixKGN2023-12-13
2820791551095681K223257Miro3D Wound MatrixKGN2022-11-21
2820791426480290K221520Miro3D Wound MatrixKGN2022-08-18
1717961354489177K143426Wound Matrix TFKGN2015-01-27
2820791359964073K143426Wound Matrix TFKGN2015-01-27
2820791782249712K134033MIROMATRIX BIOLOGICAL MESHFTM2014-03-31
1717962019040428K134033MIROMATRIX BIOLOGICAL MESHFTM2014-03-31

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
KGN72024-04-19
FTM22014-03-31

PMN#

GUDID#

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