CLARAPATH, INC.

FDA Device Registration & Listing · Hawthorne, NY, US · Registration 3023034117

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
3023034117
FEI Number
3023034117
Entity Name
CLARAPATH, INC.
City/State/Country
Hawthorne, NY, US
Establishment Address
12 Skyline Drive, Hawthorne, NY 10532, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Clarapath, Inc. (Owner Number: 10090638)
Owner / Operator Contact Address
12 Skyline Drive, Hawthorne, NY 10532, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ClaraCut ClaraTape ClaraBond SectionStar TrimStar Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IDL Microtome, Accessories Pathology Class 1 864.3010 2024-04-22
IDO Microtome, Rotary Pathology Class 1 864.3010 2024-04-22

Official Correspondent

Jessica Snyder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Clarapath, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0039-2012 Richard-Allan Scientific Company 1
Thermo Scientific Microm: Rotary Microtome: REF HM355S-3 Used for slicing tissue blocks.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3023034117. Last updated year: 2026. Please use registration number 3023034117 when referencing this establishment in official correspondence.
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