MAGBIO GENOMICS INC.

FDA Device Registration & Listing · Gaithersburg, MD, US · Registration 3013740892

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
3013740892
FEI Number
3013740892
Entity Name
MAGBIO GENOMICS INC.
City/State/Country
Gaithersburg, MD, US
Establishment Address
200 Professional Drive, Gaithersburg, MD 20879, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
MagBio Genomics Inc. (Owner Number: 10085547)
Owner / Operator Contact Address
200 Professional Drive, Gaithersburg, MD 20879, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K212113
PMA Number
N/A

All Registered Proprietary Names

MagCTL Collection Tube (Formerly MagXtract Collection Tube)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QBD Microbial Nucleic Acid Storage And Stabilization Device Microbiology Class 2 866.2950 2022-08-17

Official Correspondent

HYACINTH NTCHOBO

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MagBio Genomics Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013740892. Last updated year: 2026. Please use registration number 3013740892 when referencing this establishment in official correspondence.
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