AUTOMATED MEDICAL PRODUCTS CORP.

FDA Device Registration & Listing · Sewaren, NJ, US · Registration 2431453

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
2431453
FEI Number
2431453
Entity Name
AUTOMATED MEDICAL PRODUCTS CORP.
City/State/Country
Sewaren, NJ, US
Establishment Address
440 CLIFF RD., Sewaren, NJ 07077, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
AUTOMATED MEDICAL PRODUCTS CORP. (Owner Number: 2431453)
Owner / Operator Contact Address
440 CLIFF RD., --, Sewaren, NJ 07077, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Pediatric Liver Hook Nathanson Hook Liver Retractor Dbaly Liver Hooks Iron Intern, Hydra, Cowan Gripper, Stieber Rib Grip Kit ARH Iron Intern; Cowan Gripper; LC Greenstein Gripper; O'Brien; Stieber Rib Grip Kit; 3DSwinger(Socket); Giulianotti Kit O'Brian Lap Band Introducer O'Brian Lap Band Placer O'Brian Lap Band Closer Vaginal Retractor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FHB Hook, Gastro-Urology Gastroenterology, Urology Class 1 876.4730 2007-12-13
GAD Retractor General, Plastic Surgery Class 1 878.4800 2007-12-13
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2014-12-22
HDL Retractor, Vaginal Obstetrics/Gynecology Class 1 884.4520 2014-12-22

Official Correspondent

JANICE BROWN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AUTOMATED MEDICAL PRODUCTS CORP.
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
K922626 Andronic Devices, Ltd. ADEPT INSTRUMENT POSITIONING ACCESSORY 1992-10-19
K820290 The Anspach Effort, Inc. SELF RETAINING RETRACTOR FOR HAND SURG 1982-03-05
K760422 Cutter Laboratories, Inc. SURGICAL RETRACTOR 1976-08-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2014 Aesculap, Inc. 1
UNITRAC Pneumatic Retraction Arm. A support arm used to hold surgical instruments during surgical procedures.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2431453. Last updated year: 2026. Please use registration number 2431453 when referencing this establishment in official correspondence.
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