Madhu Instruments Pvt Ltd

FDA Device Registration & Listing · New Delhi, IN · Registration 3007317099

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
3007317099
FEI Number
3007317099
Entity Name
Madhu Instruments Pvt Ltd
City/State/Country
New Delhi, IN
Establishment Address
A-260, Okhla Industrial Area, Phase - 1, New Delhi 110020, IN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Madhu Instruments Pvt Ltd (Owner Number: 10029570)
Owner / Operator Contact Address
A-260, Okhla Industrial Area, Phase - 1, New Delhi, IN-DL 110020, IN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tearflo Madhu Madhu

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KYD Strip, Schirmer Ophthalmic Class 1 886.1800 2009-06-01
HNN Knife, Ophthalmic Ophthalmic Class 1 886.4350 2020-09-19
KYG Device, Irrigation, Ocular Surgery Ophthalmic Class 1 886.4360 2013-01-10

Official Correspondent

No official correspondent registered.

US Agent Details

DAVID ROSEN Email: drosen@foley.com Phone: (202) 6725430

Related Public Records

Same Entity

Madhu Instruments Pvt 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
K874057 Myocure, Inc. OPHTHALMIC TIP & BLADE SCALPELS 1987-12-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0026-04 Surgical Specialties Corp 1
Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024 Alcon Research LLC Aspex Facility 1
20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024 Alcon Research LLC Aspex Facility 1
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1925-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife 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 3007317099. Last updated year: 2026. Please use registration number 3007317099 when referencing this establishment in official correspondence.
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