Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2016673

FEI Number

2016673

Entity Name

Caplugs, Inc.

City/State/Country

Rancho Dominguez, CA, US

Establishment Address

18704 S Ferris Pl, Rancho Dominguez, CA 90220, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Caplugs, Inc. (Owner Number: 10050609)

Owner / Operator Contact Address

2150 Elmwood Ave, Buffalo, NY 14207, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Microscope slides & cover glass Treated plastic slides - sterile Disposable Columns Universal Columns/Mini Columns Surety Columns and Sera-Separa Columns Sputocol Sputum Collection System Collection/Transport Containers - sterile Embedding rings/processing & Embedding cassettes Hematology Dilution Vials Pipet Tips - OEM replacement Tips Transfer Pipets with Measuring Function Inoculating Loops Sterile Culture Tubes Serum sample cups Piggyback Serum Cups/transport container Disposables for use with Abbott TDx

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KEW	Slides, Microscope	Pathology	Class 1	864.3010	2015-12-08
DKO	Adsorbents, Ion-Exchange	Clinical Chemistry	Class 1	862.2230	2015-12-08
FMH	Container, Specimen, Sterile	Pathology	Class 1	864.3250	2016-10-18
KET	Filters, Cell Collection, Tissue Processing	Pathology	Class 1	864.3010	2015-12-08
JKH	Hydrazone Deriv. Of Alpha-Ketogluterate (Colorimetry), Isocitric Dehydrogen	Clinical Chemistry	Class 1	862.1420	2015-12-08
JQW	Station, Pipetting And Diluting, For Clinical Use	Clinical Chemistry	Class 1	862.2750	2015-12-08
LIB	Device, General Purpose, Microbiology, Diagnostic	Microbiology	Class 1	866.2660	2015-12-08
JJC	Analyzer, Chemistry (Sequential Multiple, Continuous Flow) Clinical Use	Clinical Chemistry	Class 1	862.2150	2015-12-08

Official Correspondent

Christine Koch

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Caplugs, 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
K851403	Ventrex Laboratories, Inc.	VENTREZYME ALLERGEN DATA REDUCTION SYSTEM	1985-06-21
K761290	Nuclear Medical Laboratories, Inc.	COMPU-PET 300	1977-02-24
K770210	G.D. Searle and Co.	ANALYTIX AUTO SAMPLE PREP. STA. 1600	1977-02-14
K760211	Instrumentation Laboratory CO	ANALYZER, GLUCOSE/UREA/CREATININE	1976-08-26

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2013	Beckman Coulter Inc.	1	COULTER PrepPlus, Part Number: 286600 Product Usage: The COULTER PrepPlus, is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.
Z-0028-2012	Beckman Coulter Inc.	1	Coulter PrepPlus 2, Part Number: 378600, Serial Numbers: 1001008698, 1001008699, and 10018700. Coulter PrePlus 2 is a microprocessor-controlled pipetting and diluting system, designed for automating sample preparation or assay methods. It is capable of aspirating and dispensing liquid samples.

Similar Registrations

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2025606	CalibreScientific US, Inc.	VANCOUVER, WA, US
1000469910	Waldemar Knittel Glasbearbeitungs GmbH	BRAUNSCHWEIG, NIEDERSACHSEN Lower Saxony, DE
1417592	MEDLINE INDUSTRIES, LP - Northfield	Northfield, IL, US
8044093	Kolplast Ci Ltda	Itupeva Sao Paulo, BR
3008496560	NINGBO GREETMED MEDICAL INSTRUMENTS CO., LTD.	Ningbo Zhejiang, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2016673. Last updated year: 2026. Please use registration number 2016673 when referencing this establishment in official correspondence.