FDA.reportPublic FDA data

Bioelectronics-Corp

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30048377023005550216BIOELECTRONICS CORPORATION1N2026-01-013880 Roundtree Rd Unit 1 Jefferson MD US 21755

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
00851329005012ActiPatch - Knee Pain Advanced Long-Lasting Relief301-874-4890brice@bielcorp.com

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
980221160312700K192234ActiPatchPQY2020-01-31
980221221733239K190251RecoveryRxILX2019-06-28
980221622238261K152432
980221539713782K022404ACTIBANDILX2002-08-08

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
ILX32019-06-28
PQY12020-01-31

PMN#

ActiPatch

2020-01-31

Bioelectronics Corporation

GUDID#