Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014680744

FEI Number

3014680744

Entity Name

ServiceSource - US Marine Corp Med Bags Program

City/State/Country

Lorton, VA, US

Establishment Address

8540 Cinder Bed Road, Suite #1500, Lorton, VA 22079, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ServiceSource, Inc, (Owner Number: 10058164)

Owner / Operator Contact Address

10467 White Granite Drive, Oakton, VA 22124, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

NSN 6545 01 624 1292 NSN 6545 01 624 0936 NSN 6545 01 624 0050 NSN 6545 01 624 0567 NSN 6545 01 549 1055 NSN 6545 01 624 0603 NSN 6545 01 624 0455 NSN 6545 01 624 0288 NSN 6545 01 624 0652 NSN 6545 01 624 0322 NSN 6545 01 624 1270 NSN 6545 01 624 0339 NSN 6545 01 624 1358 NSN 6545 01 624 0500 NSN 6545 01 624 0075 NSN 6545 01 624 0134 NSN 6545 01 624 0232 NSN 6545 01 624 0993 NSN 6545 01 624 0462 NSN 6545 01 624 0881

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OFQ	Anesthesia Kit	Anesthesiology	Class 2	868.5120	2018-07-19
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2018-07-19
LRO	General Surgery Tray	General, Plastic Surgery	Class 2	878.4370	2018-07-19
OVN	Suture Kit	General, Plastic Surgery	Class 2	878.4830	2018-07-19

Official Correspondent

Michael Jordan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ServiceSource, Inc,

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
K961683	J.J. Skinner, Inc.	JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAY	1996-05-10

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0028-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil ENT Pack REF AMS9977 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0030-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical T and A Pack REF AMS11482 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0031-2025	Windstone Medical Packaging, Inc.	2	Aligned Medical Tonsil Pack REF AMS14809 that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a convenient manner for use in a general clinical procedure.
Z-0095-2021	Alcon Research, LLC	2	Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product Usage: used by ophthalmic surgeons in a variety of ophthalmic surgeries.

Similar Registrations

Registration Number	Establishment Name	Location
1047429	AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY 305	TOANO, VA, US
1030451	MEDICAL ACTION INDUSTRIES, INC. 306	ARDEN, NC, US
3007329020	Cardinal Health 200, LLC	El Paso, TX, US
3005012805	MIDWEST STERILIZATION CORP.	LAREDO, TX, US
1928237	MIDWEST STERILIZATION CORP.	JACKSON, MO, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014680744. Last updated year: 2026. Please use registration number 3014680744 when referencing this establishment in official correspondence.