Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3001452053

FEI Number

3001452053

Entity Name

SERVICE GRAPHICS, INC.

City/State/Country

INDIANAPOLIS, IN, US

Establishment Address

8350 ALLISON AVE., INDIANAPOLIS, IN 46268, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

SERVICE GRAPHICS, INC. (Owner Number: 9052909)

Owner / Operator Contact Address

8350 ALLISON AVE., --, Indianapolis, IN 46268, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K931258

PMA Number

N/A

All Registered Proprietary Names

Blood Collection Vial ACCU-CHEK Softclix

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIM	Tubes, Vacuum Sample, With Anticoagulant	Clinical Chemistry	Class 2	862.1675	2025-04-28
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2025-04-28
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2011-06-22

Official Correspondent

BILL PRICE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SERVICE GRAPHICS, 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
K945777	Smiths Industries Medical Systems, Inc.	PRO-VENT(TM), PULSATOR(R), AND LINE DRAW(TM) ARTERIAL BLOOD SAMPLING SYRINGES	1994-12-22
K130132	Medipurpose Pte. , Ltd.	BABYLANCE HEEL INCISION DEVICE	2013-02-11

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.
Z-0044-2008	Becton Dickinson & Company	2	Microtainer Safety Flow Lancets; Green Sterile, Use Once and Discard; 1.4 mm Blade Length; 1.0mm Blade Width; Becton Dickinson Vacutainer Systems; Becton Dickinson & Company; Franklin Lakes, NJ 07417

Similar Registrations

Registration Number	Establishment Name	Location
1921846	Cardinal Health	Hazelwood, MO, US
1917413	BECTON, DICKINSON & CO.	BROKEN BOW, NE, US
1061124	Sterigenics U.S., LLC	Charlotte, NC, US
2029015	Sterigenics U.S., LLC	Ontario, CA, US
9617032	Becton, Dickinson & Company (BD)	Plymouth Devon, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001452053. Last updated year: 2026. Please use registration number 3001452053 when referencing this establishment in official correspondence.