Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003860739

FEI Number

3003860739

Entity Name

MEDI INSTRUMENTS INC.

City/State/Country

Scarsdale, NY, US

Establishment Address

14 Garth Rd, Scarsdale, NY 10583, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

MEDI INSTRUMENTS INC. (Owner Number: 9051689)

Owner / Operator Contact Address

14 Garth Road, Scarsdale, NY 10583, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MEDI INSTRUMENTS medi instruments inc medi instruments inc OPHTHALMIC BAR PRISM MEDI INSTRUMENTS MEDI INSTRUMENTS medi instruments inc SCHIRMER STRIP medi instruments inc MEDI INSTRUMENT INC MEDI INSTRUMENTS MEDI INSTRUMENTS medi instruments inc MEDI INSTRUMENTS MEDI INSTRUMENTS MANUAL OPHTHALMIC TREPHINE medi instruments inc MEDI INSTRUMENTS INC.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HND	Spatula, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HNQ	Hook, Ophthalmic	Ophthalmic	Class 1	886.4350	2017-12-29
HKW	Prism, Bar, Ophthalmic	Ophthalmic	Class 1	886.1650	2006-09-08
HNR	Forceps, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HNF	Scissors, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
KYD	Strip, Schirmer	Ophthalmic	Class 1	886.1800	2006-09-08
HNB	Spoon, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
GAD	Retractor	General, Plastic Surgery	Class 1	878.4800	2014-12-04
HNZ	Curette, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HNC	Specula, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HOE	Caliper, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HNA	Spud, Ophthalmic	Ophthalmic	Class 1	886.4350	2004-03-01
HRH	Trephine, Manual, Ophthalmic	Ophthalmic	Class 1	886.4350	2006-09-08
HNM	Needle, Ophthalmic Suturing	Ophthalmic	Class 1	886.4350	2014-12-16

Official Correspondent

PUJA MEHTA

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

MEDI INSTRUMENTS INC.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3003860763	BILINK INTERNATIONAL INC.	JODHPUR Rajasthan, IN

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.

Similar Registrations

Registration Number	Establishment Name	Location
1045379	STEPHENS INSTRUMENTS, INC	LEXINGTON, KY, US
3012267976	SURGIPROS LLC	Palmetto, FL, US
3011137372	Teleflex Medical LLC	Morrisville, NC, US
3003553186	66 VISION TECH CO., LTD.	Suzhou Jiangsu, CN
1123010	TRINITY STERILE, INC.	SALISBURY, MD, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003860739. Last updated year: 2026. Please use registration number 3003860739 when referencing this establishment in official correspondence.