Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015715780

FEI Number

3015715780

Entity Name

LEGACY BIOLOGICALS

City/State/Country

Baltimore, MD, US

Establishment Address

6260 Frankford Ave, Baltimore, MD 21206, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Legacy Biologicals (Owner Number: 10061031)

Owner / Operator Contact Address

6260 Frankford Ave, Baltimore, MD 21206, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media Legacy Culture Media

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JSC	Culture Media, General Nutrient Broth	Microbiology	Class 1	866.2350	2019-08-01
JSB	Culture Media, Vitamin Assay	Microbiology	Class 1	866.2350	2019-08-01
JSD	Culture Media, Selective Broth	Microbiology	Class 1	866.2360	2019-08-01
JSF	Culture Media, Single Biochemical Test	Microbiology	Class 1	866.2320	2019-08-01
JTR	Kit, Quality Control For Culture Media	Microbiology	Class 1	866.2480	2019-08-01
KIT	Media And Components, Synthetic Cell And Tissue Culture	Hematology	Class 1	864.2220	2019-08-01
JSI	Culture Media, Selective And Differential	Microbiology	Class 1	866.2360	2019-08-01
JSE	Culture Media, Multiple Biochemical Test	Microbiology	Class 1	866.2320	2019-08-01
KZI	Culture Media, Enriched	Microbiology	Class 1	866.2330	2019-08-01
JSJ	Culture Media, Selective And Non-Differential	Microbiology	Class 1	866.2360	2019-08-01
JSH	Culture Media, Non-Selective And Differential	Microbiology	Class 1	866.2320	2019-08-01

Official Correspondent

Robin Williams

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Legacy Biologicals

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
K790620	Anaerobe Systems	LOMBARD DOWELL BROTH MEDIUMW/TH REONINE	1979-04-23
K811056	Acumedia Manufacturers, Inc.	BRAIN HEART INFUSION	1981-04-29
K822995	Granite Diagnostics, Inc.	ANDRADES FERMENTATION MEDIA	1982-11-16
K880126	Hardy Media	LAURYL TRYPTOSE BROTH	1988-03-31
K821594	Hardy Media	UREA AGAR SLANT	1982-07-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0024-05	Remel, Inc.	1	Remel Chocolate Agar, catalog #01301, containing 15 plates/pkg, for in-vitro diagnostic use. The firm name on the label is Remel, Lenexa, KS.

Similar Registrations

Registration Number	Establishment Name	Location
1119779	BECTON, DICKINSON & CO.	SPARKS, MD, US
3027341451	JIAOYUE PHARMACEUTICAL (HUIZHOU) CO.LTD	Huizhou Guangdong, CN
3009547954	Hardy Diagnostics	Springboro, OH, US
2016672	KEY SCIENTIFIC PRODUCTS	Stamford, TX, US
9680687	CHROMAGAR	Saint-Denis Seine-Saint-Denis, FR

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015715780. Last updated year: 2026. Please use registration number 3015715780 when referencing this establishment in official correspondence.