BELAIR INSTRUMENT CO, LLC D/B/A AVANTIK

FDA Device Registration & Listing · Pine Brook, NJ, US · Registration 3014680809

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
3014680809
FEI Number
3014680809
Entity Name
BELAIR INSTRUMENT CO, LLC D/B/A AVANTIK
City/State/Country
Pine Brook, NJ, US
Establishment Address
19 Chapin Road, Building C, Pine Brook, NJ 07058, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Belair Instrument Co, LLC d/b/a Avantik (Owner Number: 10057530)
Owner / Operator Contact Address
19 Chapin Road, Building C, Pine Brook, NJ 07058, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Avantik Tissue Floatation Bath Avantik VTM-Kit Avantik VTM Avantik QS12 Cryostat Sante Pipette Tips Avantik Pipette Tip

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IDY Bath, Flotation, Tissue Pathology Class 1 864.3010 2025-01-16
JSK Supplement, Culture Media Microbiology Class 1 866.2450 2020-11-16
KEW Slides, Microscope Pathology Class 1 864.3010 2018-05-30
KES Coverslips, Microscope Slide Pathology Class 1 864.3010 2018-05-30
IDP Microtome, Cryostat Pathology Class 1 864.3010 2021-05-27
IDL Microtome, Accessories Pathology Class 1 864.3010 2018-05-30
JRC Micro Pipette Clinical Chemistry Class 1 862.2050 2021-12-16
IDZ Cassettes, Tissue Pathology Class 1 864.3010 2018-05-30

Official Correspondent

Carl Suraci

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Belair Instrument Co, LLC d/b/a Avantik
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014680809. Last updated year: 2026. Please use registration number 3014680809 when referencing this establishment in official correspondence.
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