APPASAMY OCULAR DEVICES (P) LTD.

FDA Device Registration & Listing · Puducherry, IN · Registration 3003591781

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
3003591781
FEI Number
3003591781
Entity Name
APPASAMY OCULAR DEVICES (P) LTD.
City/State/Country
Puducherry, IN
Establishment Address
R.S.No.9/1,2&3, NH 45A, Villupuram Main Road,, Vadamangalam,, Puducherry 605102, IN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
APPASAMY OCULAR DEVICES (P) LTD. (Owner Number: 9048612)
Owner / Operator Contact Address
R.S.No.9/1,2&3, NH 45A, Villupuram Main Road,, Vadamangalam,, Puducherry, IN-PY 605102, IN
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
KYB Lens, Guide, Intraocular Ophthalmic Class 1 886.4300 2014-10-28

Official Correspondent

ARVIND KASTHURI

US Agent Details

Jayesh Patel Business: Amstermed Inc Email: info@amstermed.nl Phone: (714) 5954919

Related Public Records

Same Entity

APPASAMY OCULAR DEVICES (P) 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
K823222 American Medical Optics INTRAOCULAR LENS GUIDE 1982-12-28

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0835-2025 Alcon Research LLC 1
Brand Name: Alcon Product Name: Monarch III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description: Monarch III D delivery cartridge Lens Guide, Intraocular Component: N/A

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003591781. Last updated year: 2026. Please use registration number 3003591781 when referencing this establishment in official correspondence.
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