Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009561706

FEI Number

3009561706

Entity Name

UPSTREAM PERIPHERAL TECHNOLOGIES LTD.

City/State/Country

Caesarea Central, IL

Establishment Address

43 Haeshel st. ARAN building, P.O.B. 3067, Caesarea Central 3088900, IL

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Upstream peripheral Technologies ltd. (Owner Number: 10060819)

Owner / Operator Contact Address

43 Haeshel st. ARAN building, P.O.B. 3067, Caesarea, IL-M 3088900, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GoBack Crossing Catheter , BeBack Crossing Catheter

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
PDU	Catheter For Crossing Total Occlusions	Cardiovascular	Class 2	870.1250	2022-09-21

Official Correspondent

Dan Rottenberg

US Agent Details

Jacob Offenberger Email: jacoboffenberger@hotmail.com Phone: (818) 5153700

Related Public Records

Same Entity

Upstream peripheral Technologies ltd.

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
K071227	Spectranetics Corp.	CLIRPATH TURBO EXCIMER LASER CATHETER (RX) -0.9MM, (RX) -1.4MM, (RX) -1.7MM, (RX) -2.0MM, MODEL 310-154, 314-159, 317-15	2007-07-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009561706. Last updated year: 2026. Please use registration number 3009561706 when referencing this establishment in official correspondence.