Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1840727618
Device Listing 1840727618
Listing Summary
#
Listing key
1840727618
Premarket submission
K201827
Device
GR-17 Resin System
Applicant
Pro3Dure Medical GmbH
Product code
EBG
Decision date
2020-11-05
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
227105
3014888923
3014888923
PRO3DURE MEDICAL GMBH
1
N
2026-01-01
Am Burgberg 13 Iserlohn North Rhine-Westphalia DE 58642