INSTAPATH INC.

FDA Device Registration & Listing · Houston, TX, US · Registration 3016418391

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
3016418391
FEI Number
3016418391
Entity Name
INSTAPATH INC.
City/State/Country
Houston, TX, US
Establishment Address
2450 Holcombe Blvd Ste J, Houston, TX 77021, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Instapath Inc. (Owner Number: 10090906)
Owner / Operator Contact Address
2450 Holcombe Blvd Ste J, Houston, TX 77021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nova

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IBK Microscope, Fluorescence/U.V. Pathology Class 1 864.3600 2024-05-30

Official Correspondent

David Tulman

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Instapath Inc.
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 3016418391. Last updated year: 2026. Please use registration number 3016418391 when referencing this establishment in official correspondence.
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