ANTHONY PRODUCTS, INC.

FDA Device Registration & Listing · Indianapolis, IN, US · Registration 1824037

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
1824037
FEI Number
1824037
Entity Name
ANTHONY PRODUCTS, INC.
City/State/Country
Indianapolis, IN, US
Establishment Address
7740 RECORDS ST, Indianapolis, IN 46226, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Anthony Products, Inc. (Owner Number: 10025507)
Owner / Operator Contact Address
7740 Records Street, Indianapolis, IN 46226, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K002257
PMA Number
N/A

All Registered Proprietary Names

GEAC TIP

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRW Scissors, General, Surgical General, Plastic Surgery Class 1 878.4800 2017-02-10
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2013-02-05

Official Correspondent

Jeremy Borden

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Anthony Products, Inc.
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
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

Similar Registrations

Registration Number Establishment Name Location
8010298 RUDOLF MEDICAL GMBH + CO. KG FRIDINGEN Baden-Wurttemberg, DE
8043496 REDA INSTRUMENTE GMBH TUTTLINGEN Baden-Wurttemberg, DE
8040373 NADEEM SURGICAL CORP. PRIVATE LTD. SIALKOT Punjab, PK
2531475 URAMIX, INC. E Lansdowne, PA, US
1417592 MEDLINE INDUSTRIES, LP - Northfield Northfield, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1824037. Last updated year: 2026. Please use registration number 1824037 when referencing this establishment in official correspondence.
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