Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019946783

FEI Number

3019946783

Entity Name

RETROPERC, INC.

City/State/Country

Jersey City, NJ, US

Establishment Address

111 Town Square Pl Ste 1203, Jersey City, NJ 07310, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

RetroPerc, Inc. (Owner Number: 10082484)

Owner / Operator Contact Address

32 Pleasant Ave, Passaic, NJ 07055, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K160077

PMA Number

N/A

All Registered Proprietary Names

RetroPerc

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LJE	Catheter, Nephrostomy	Unknown	Class U	N/A	2021-08-03

Official Correspondent

Jason Wynberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RetroPerc, 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 3019946783. Last updated year: 2026. Please use registration number 3019946783 when referencing this establishment in official correspondence.