Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2245437

FEI Number

2245437

Entity Name

E-BEAM SERVICES, INC.

City/State/Country

CRANBURY, NJ, US

Establishment Address

118 Melrich Rd, CRANBURY, NJ 08512, US

Establishment Type(s)

Sterilize Medical Device for Another Party (Contract Sterilizer)

Owner / Operator

E-BEAM Services, Inc. (Owner Number: 9038519)

Owner / Operator Contact Address

118 Melrich Road, --, Cranbury, NJ 08512, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GammaTile PREVENTOGEN Catrix Wound Dressing Repliderm Wound Dressing

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2012-12-28
KXK	Source, Brachytherapy, Radionuclide	Radiology	Class 2	892.5730	2025-09-02
KDT	Container, Specimen Mailer And Storage, Sterile	Pathology	Class 1	864.3250	2012-11-26
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2023-08-16
KGN	Wound Dressing With Animal-Derived Material(S)	Unknown	Class U	N/A	2015-02-12

Official Correspondent

Brianna Wong

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

E-BEAM Services, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
1531062	E-BEAM SERVICES, INC.	LEBANON, OH, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K945777	Smiths Industries Medical Systems, Inc.	PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES	1994-12-22
K112888	Kensey Nash Corporation	MESO WOUND MATRIX	2012-02-10
K040211	Collagen Matrix, Inc.	MODIFICATION TO: COLLAGEN TOPICAL WOUND DRESSING	2004-02-27

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0030-2014	Perkin Elmer Health Sciences, Inc.	2	Perkin Elmer 226 Sample Collection Device, Serial numbers: 06132903 - 06198900. The PerkinElmer 226 Sample Collection Devices are intended to be used as a medium to collect and transport whole blood specimen spots to a laboratory, in newborn screening. The device includes a tear-apart form for the collection of demographic information.

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1423507	CAREFUSION 2200, INC.	Vernon Hills, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2245437. Last updated year: 2026. Please use registration number 2245437 when referencing this establishment in official correspondence.