Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020831613

FEI Number

3020831613

Entity Name

KASHI SCIENTIFIC LLC

City/State/Country

Portland, OR, US

Establishment Address

5020 SW View Point Terr, Portland, OR 97239, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Kashi Scientific LLC (Owner Number: 10083194)

Owner / Operator Contact Address

5020 SW View Point Terr, Portland, OR 97239, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K093910

PMA Number

N/A

All Registered Proprietary Names

Sterile, Disposable, Specimen Collection Flocked Swab Sterile, Disposable, Specimen Collection Nasopharyngeal Swab Disposable Cytology Brush Universal Viral Transport Medium Kit Powder-Free Nitrile Examination Gloves Conventional Holder - General Type Safety Holder with Safety Shield Blood Collection Set With Pre-Attached Holder Universal Pipette Tips CULTURE MEDIA, NON-SELECTIVE AND NON-DIFFERENTIAL Disposable Sampling Tube Gel & Clot Activator Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2021-11-01
JSF	Culture Media, Single Biochemical Test	Microbiology	Class 1	866.2320	2021-11-18
LZA	Polymer Patient Examination Glove	General Hospital	Class 1	880.6250	2022-01-17
KST	System, Blood Collection, Vacuum-Assisted, Manual	Hematology	Class 1	864.9125	2022-05-12
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2022-03-29
BTP	Dropper, Ether	Anesthesiology	Class 1	868.5420	2023-12-28
JSG	Culture Media, Non-Selective And Non-Differential	Microbiology	Class 1	866.2300	2022-01-05
JKA	Tubes, Vials, Systems, Serum Separators, Blood Collection	Clinical Chemistry	Class 2	862.1675	2022-03-29

Official Correspondent

Kamyar Kashi

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Kashi Scientific LLC

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
K822995	Granite Diagnostics, Inc.	ANDRADES FERMENTATION MEDIA	1982-11-16
K880126	Hardy Media	LAURYL TRYPTOSE BROTH	1988-03-31
K821594	Hardy Media	UREA AGAR SLANT	1982-07-08
K212801	Hong Seng Gloves Sdn Bhd	Powder free nitrile examination glove- black, non sterile	2022-01-09
K260806	Vista Industries,, LLC	Nitrile Disposable Examination Gloves	2026-06-03

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796
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
3032760064	CARAN PRECISION ENGINEERING & MANUFACTURING CORP.	Brea, CA, US
3015505238	CITOTEST SCIENTIFIC CO.,LTD.	Nanjing Jiangsu, CN
3014159736	VIETNAM MEDICAL PLASTIC JSC	Tam Diep Ward Ninh Binh, VN
3009656988	STERIPACK USA (LIMITED) LLC	Lakeland, FL, US
3010407203	Sterigenics Italy SpA	Minerbio Bologna, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020831613. Last updated year: 2026. Please use registration number 3020831613 when referencing this establishment in official correspondence.