KURIN, INC.

FDA Device Registration & Listing · San Diego, CA, US · Registration 3013696225

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013696225
FEI Number
3013696225
Entity Name
KURIN, INC.
City/State/Country
San Diego, CA, US
Establishment Address
10840 Thornmint Road, Suite 111, San Diego, CA 92127, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Kurin, Inc. (Owner Number: 10057862)
Owner / Operator Contact Address
10840 Thornmint Road, Suite 111, San Diego, CA 92127, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K220677
PMA Number
N/A

All Registered Proprietary Names

Kurin Blood Collection Set w/ Kurin Lock Tech - D-11221/D-11223/M-11221/M-11223/T-11221/T-11223 Kurin Blood Collection Set w/ Jet Lock Tech - DJ-121/DJ-123/MJ-121/MJ-123/TJ-121/TJ-123 Kurin Blood Collection Set w/ Jet Lock Tech - DJ-221/DJ-223/MJ-221/MJ-223/TJ-221/TJ-223 Kurin Blood Collection Set w/ Kurin Lock Tech - D-21221/D-21223/M-21221/M-21223/T-21221/T-21223 Kurin Blood Collection Set w/ Jet Lock (w/o extension set) - DJ-PIV12/MJ-PIV12/TJ-PIV12/SJ-PIV10 Kurin Blood Collection Set w/ Jet Lock Tech (w/ extension set) - DJ-PIV18/MJ-PIV18/TJ-PIV18/SJ-PIV10 Kurin Blood Collection Set w/ Kurin Lock Tech (w/o extension set) - D-PIV12/M-PIV12/T-PIV12/S-PIV Kurin Blood Collection Set w/ Kurin Lock Tech (w/ extension set) - D-PIV18/M-PIV18/T-PIV18/S-PIV10 Kurin Blood Collection Set w/ Jet Lock Tech (w/o extension set) - DJ-PIV12/MJ-PIV12/TJ-PIV12/SJ-PIV4 Kurin Blood Collection Set w/ Kurin Lock Tech (w/ extension set) - D-PIV18/M-PIV18/T-PIV18/S-PIV10 Kurin Blood Collection Set w/ Jet Lock Tech (Venipuncture/Push-Button) - DJ-221/DJ-223/MJ-221/MJ-223/TJ-221/TJ-223 Kurin Blood Collection Set w/ Kurin Lock Tech (Venipuncture/Slide) - D-11221/D-11223/M-11221/M-11223/T-11221/T-11223 Kurin Blood Collection Set w/ Jet Lock Tech (Venipuncture/Slide)-DJ-121/DJ-123/MJ-121/MJ-123/TJ-121/TJ-123 Kurin Blood Collection Set w/ Jet Lock Tech (w/ extension set) - DJ-PIV18/MJ-PIV18/TJ-PIV18/SJ-PIV10 Kurin Blood Collection Set w/ Kurin Lock Tech (Venipuncture/Push-Button) - D-21221/D-21223/M-21221/M-21223/T-21221/T-212 Kurin Blood Collection Set w/ Kurin Lock Tech (w/o extension set) - D-PIV12/M-PIV12/T-PIV12/S-PIV4

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 2018-06-04
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection Clinical Chemistry Class 2 862.1675 2024-06-07
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection Clinical Chemistry Class 2 862.1675 2019-08-19
FPA Set, Administration, Intravascular General Hospital Class 2 880.5440 2019-08-19
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection Clinical Chemistry Class 2 862.1675 2026-01-08
FPA Set, Administration, Intravascular General Hospital Class 2 880.5440 2026-01-08

Official Correspondent

Nealen Hartman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kurin, 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
K221518 Np Medical NP Medical nCompass Extension Set with Stabilizing Base 2022-11-03
K953474 Medikmark, Inc. IV START KIT 1995-10-02
K972493 Nipro Medical Corp. NIPRO DISPOSABLE SOLUTION INFUSION SET 1997-09-18
K982672 Baxter Healthcare Corp COLLEAGUE PUMP SYRINGE ADAPTER SET 1998-09-04

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-0010-2025 Smiths Medical ASD Inc. 2
CADD Medication Cassette Reservoir, 100mL, Product Code 21-7002-24
Z-0011-2025 Smiths Medical ASD Inc. 2
CADD Medication Cassette Reservoir, 100mL, FS, Product Code 21-7302-24
Z-0012-2013 Baxter Healthcare Corp. Rt. 2
Baxter Interlink System Buretrol Solution Set with 150 mL Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access device.
Z-0012-2025 Smiths Medical ASD Inc. 2
CADD Medication Cassette Reservoir, 100mL, FS, YELLOW, Product Code 21-7300-24

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013696225. Last updated year: 2026. Please use registration number 3013696225 when referencing this establishment in official correspondence.
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