Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3033526648

FEI Number

3033526648

Entity Name

SURGIMED DEVICES

City/State/Country

AHMEDABAD Gujarat, IN

Establishment Address

349, SAHITYA INDUSTRIAL HUB, BAKROL-BUJARANG ROAD. BAKROL, AHMEDABAD Gujarat 382430, IN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SURGIMED DEVICES (Owner Number: 10091560)

Owner / Operator Contact Address

B-10, GIRIVAR BUNGLOW, NEAR SWAMINARAYAN GURUKUL, NIRAT CROSS ROAD. VASTRAL, AHMEDABAD, IN-GJ 382418, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SURGIMED Eye shield Ophthalmic Knife Chisel Blade Myringotomy Blade/ Knife SURGIMED Ophthalmic surgical instruments Curette Dermal OPHTHALMIC CANNULAS SURGIMED Eye pad

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2025-02-24
HNN	Knife, Ophthalmic	Ophthalmic	Class 1	886.4350	2024-10-15
GES	Blade, Scalpel	General, Plastic Surgery	Class 1	878.4800	2024-10-15
JYP	Knife, Myringotomy	Ear, Nose, Throat	Class 1	874.4420	2024-10-15
KDC	Instrument, Surgical, Disposable	General, Plastic Surgery	Class 1	878.4800	2025-02-24
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2024-10-15
HMX	Cannula, Ophthalmic	Ophthalmic	Class 1	886.4350	2024-10-15
HMP	Pad, Eye	General, Plastic Surgery	Class 1	878.4440	2025-02-24

Official Correspondent

No official correspondent registered.

US Agent Details

Manoj Zacharias Business: Liberty Management Group Ltd. Email: office@libertymanagement.us Phone: (630) 2702921

Related Public Records

Same Entity

SURGIMED DEVICES

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
K831798	I M, Inc.	DISPOSABLE SCALPELS	1983-07-19
K854401	Microsurgical Technology, Inc.	THE NEW MOBILE TIP MCINTYRE CANNULA	1985-12-30

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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3021343301	TAIZHOU YIZHAN OPTICAL GLASSES CO., LTD	Taizhou City Zhejiang, CN
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033526648. Last updated year: 2026. Please use registration number 3033526648 when referencing this establishment in official correspondence.