Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017923561

FEI Number

3017923561

Entity Name

SARIS AND THINGS, INC.

City/State/Country

Plainfield, IL, US

Establishment Address

24119 W Riverwalk Ct., Unit 131, Plainfield, IL 60544, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Saris and Things, Inc. (Owner Number: 10080196)

Owner / Operator Contact Address

24119 W Riverwalk Ct., Unit 131, Plainfield, IL 60544, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K223201

PMA Number

N/A

All Registered Proprietary Names

Whatman ADX100 Medline Medline Polymedco BD OWEN MUMFORD INC Unistik OWEN MUMFORD INC BD SNT Biotech Medline Unistik

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OIB	Blood And Urine Collection Kit (Excludes Hiv Testing)	Pathology	Class 1	864.3250	2024-05-24
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2024-05-24
OOX	Automated Occult Blood Analyzer	Hematology	Class 2	864.6550	2023-11-01
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2024-05-24
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2024-05-24
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2024-05-24
FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature	General, Plastic Surgery	Class 2	878.4850	2024-05-24

Official Correspondent

Shital Daftari

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
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
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.

Similar Registrations

Registration Number	Establishment Name	Location
1420054	LSL HEALTHCARE	Niles, IL, US
1047429	AVID MEDICAL, INC. A MEDICAL ACTION IND. COMPANY 305	TOANO, VA, US
3006191977	AERO-MED LLC	East Hartford, CT, US
1824619	CENTURION MEDICAL PRODUCTS, LP	HOWELL, MI, US
1060680	DeRoyal Industries, Inc.	NEW TAZEWELL, TN, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017923561. Last updated year: 2026. Please use registration number 3017923561 when referencing this establishment in official correspondence.