FDA.reportPublic FDA data

BIOLUX TECHNOLOGY GMBH

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30172711313017271131BIOLUX TECHNOLOGY GMBH1N2026-01-01Neubaugasse 31 Absdorf Niederosterreich AT 3462

GUDID Contact Samples#

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

Source GUDID, Product, Phone table
Source GUDIDProductPhoneEmail
09120118090029OrthoPulse - OPi8886690674support@orthopulse.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2913261898147490K230905OrthoPulse 2.0E (OPi2E-100)PLH2023-06-09
2913261974186863K143120OrthoPulsePLH2015-07-24

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
PLH22023-06-09

PMN#

GUDID#