KRENERB, LLC

FDA Device Registration & Listing · Hockessin, DE, US · Registration 3031464228

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3031464228
FEI Number
3031464228
Entity Name
KRENERB, LLC
City/State/Country
Hockessin, DE, US
Establishment Address
503 Wilson Dr, Hockessin, DE 19707, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device,Manufacture Medical Device
Owner / Operator
Krenerb, LLC (Owner Number: 10090997)
Owner / Operator Contact Address
503 Wilson Dr, Hockessin, DE 19707, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K160323
PMA Number
N/A

All Registered Proprietary Names

FlowKeepers

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter Neurology Class 2 882.5890 2024-06-12
NGX Stimulator, Muscle, Powered, For Muscle Conditioning Physical Medicine Class 2 890.5850 2024-06-12

Official Correspondent

Joachim Berkner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Krenerb, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K221200 Xbody Hungary Kft. XBody Go USA, XBody Pro USA 2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031464228. Last updated year: 2026. Please use registration number 3031464228 when referencing this establishment in official correspondence.
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