JACOBS INSTITUTE, INC.

FDA Device Registration & Listing · Buffalo, NY, US · Registration 3012595935

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
3012595935
FEI Number
3012595935
Entity Name
JACOBS INSTITUTE, INC.
City/State/Country
Buffalo, NY, US
Establishment Address
875 Ellicott St., 5th Floor, Buffalo, NY 14203, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Jacobs Institute, Inc. (Owner Number: 10060204)
Owner / Operator Contact Address
875 Ellicott St., 5th Floor, Buffalo, NY 14203, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PTL Wire, Guide, Catheter, Exempt Cardiovascular Class 2 870.1330 2019-04-10

Official Correspondent

Kevin Lawson

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Jacobs Institute, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012595935. Last updated year: 2026. Please use registration number 3012595935 when referencing this establishment in official correspondence.
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