Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006389770

FEI Number

3006389770

Entity Name

MEDITEC DEVICES

City/State/Country

VASAI(E), THANE, MAHARASHTRA, IN

Establishment Address

2A MITUL IND. ESTATE,, SATIVALI ROAD,, VASAI(E), THANE, MAHARASHTRA 401208, IN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

MEDITEC DEVICES (Owner Number: 9096299)

Owner / Operator Contact Address

A201 GREG MARSH RESIDENCY, NEAR MADHUBAN TOWNSHIP, GOKHIVARE,, VASAI EAST,DISTRICT PALGHAR, IN-MH 401208, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Target Point Kevorkian Remover Intrauterine Device Hook Type Gynex Keye's Punch Tru-Punch-Sklar NA Safety Scalpel Canister Sterile Vaccum Tubing Set 1 Scope Display Case (disposable) 1 Scope HD Blade(disposable) Uterine Sound Phem Alert COMFORT FIT MONASCOPE Tickle Lipo Sleeve for Cannula Robertazzi Dennis Dilators Soft Dilators other non proprietary Earwell

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HFB	Forceps, Biopsy, Gynecological	Obstetrics/Gynecology	Class 1	884.4530	2015-07-16
HCY	Curette, Uterine	Obstetrics/Gynecology	Class 1	884.4530	2026-03-10
HHF	Remover, Intrauterine Device, Contraceptive, Hook-Type	Obstetrics/Gynecology	Class 1	884.4530	2020-02-05
EME	Punch, Biopsy, Surgical	Dental	Class 1	872.4565	2026-03-10
GBI	Material, External Aesthetic Restoration, Used With Adhesive	General, Plastic Surgery	Class 1	878.3800	2017-02-27
GES	Blade, Scalpel	General, Plastic Surgery	Class 1	878.4800	2016-02-24
KDQ	Bottle, Collection, Vacuum	General Hospital	Class 2	880.6740	2020-08-21
FCZ	Tube, Smoke Removal, Endoscopic	Gastroenterology, Urology	Class 1	876.1500	2025-12-22
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2024-08-04
HHM	Sound, Uterine	Obstetrics/Gynecology	Class 1	884.4530	2016-07-19
LNW	Paper, Obstetric Ph	Clinical Chemistry	Class 1	862.1550	2011-01-21
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2007-01-29
FGY	Cannula, Injection	General, Plastic Surgery	Class 1	878.4200	2025-07-28
BTQ	Airway, Nasopharyngeal	Anesthesiology	Class 1	868.5100	2013-03-11
HDQ	Dilator, Cervical, Fixed Size	Obstetrics/Gynecology	Class 1	884.4530	2011-03-14
GDF	Guide, Needle, Surgical	General, Plastic Surgery	Class 1	878.4800	2026-03-10
FTN	Plastic Surgery And Accessories Kit	General, Plastic Surgery	Class 1	878.3925	2013-03-11

Official Correspondent

SAJJAN PAUL

US Agent Details

SANJAY SHONEY Business: SHONEY SCIENTIFIC INC. Email: Shoney53186@yahoo.com Phone: (262) 9700170

Related Public Records

Same Entity

MEDITEC DEVICES

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0012-2008	Becton Dickinson & Company	1	Shelf Pack: Bard-Parker Rib-Back Carbon Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417
Z-0013-2008	Becton Dickinson & Company	1	Shelf Pack: Bard-Parker Rib-Back Stainless Steel no.11, surgical blade. Unit Package: Contents of unopened or undamaged package guaranteed sterile; After use place product in a puncture resistant container and dispose properly. Becton Dickinson Becton Dickinson Acute Care Franklin Lakes, NJ 07417
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006389770. Last updated year: 2026. Please use registration number 3006389770 when referencing this establishment in official correspondence.