FDA.reportPublic FDA data

Demetra, Inc.

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30241241723024124172Demetra, Inc.1N2026-01-0143 Broad St Ste B403 Hudson MA US 01749
30402668253040266825DEMETRA, INC.1N2026-01-016800 Poplar Ave Ste 120 Germantown TN US 38138

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3425611514801539K222903Tailored-H Cervical Stand Alone SystemOVE2022-11-18
3089421136389023K212962TRELLIS™ SI Joint Fusion SystemOUR2022-04-11
3425611965662926K200458Tailored-C Cervical Interbody Fusion SystemODP2020-12-28
3425611020738361
3089421603253098
3425611680387250
3425611757418626
3425611903972986

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
OVE12022-11-18
OUR12022-04-11
ODP12020-12-28

GUDID#