DUOPROSS MEDITECH CORPORATION

FDA Device Registration & Listing · FARMINGDALE, NY, US · Registration 3003681915

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
3003681915
FEI Number
3003681915
Entity Name
DUOPROSS MEDITECH CORPORATION
City/State/Country
FARMINGDALE, NY, US
Establishment Address
154 Marine St, FARMINGDALE, NY 11735, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
DUOPROSS MEDITECH CORP (Owner Number: 9055828)
Owner / Operator Contact Address
154 Marine Street, Farmingdale, NY 11735, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

safetytray bak'snap insosafe safetytray insosafe bak'snap DPS safetytray insosafe bak'snap bak'snap safetytray insosafe DPS safetytray insosafe bak'snap DPS DPS safetytray insosafe bak'snap baksnap

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-04-24
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-04-24
FMF Syringe, Piston General Hospital Class 2 880.5860 2017-04-24
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-04-24
FMF Syringe, Piston General Hospital Class 2 880.5860 2025-12-22
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2017-07-21
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-07-21
FPD Tube, Feeding Gastroenterology, Urology Class 2 876.5980 2017-04-24
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-04-24
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2017-04-24
FMF Syringe, Piston General Hospital Class 2 880.5860 2017-04-24
MEG Syringe, Antistick General Hospital Class 2 880.5860 2017-04-24
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2017-04-24

Official Correspondent

VINCENT FU

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DUOPROSS MEDITECH CORP
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
K092413 Inviro Medical Devices, Inc. INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES 2009-09-04
K163162 Jiangxi Hongda Medical Equipment Group , Ltd. Sterile Hypodermic Safety Syringes for Single Use 2017-03-20
K880350 Honway International Co. YUE/FA DISPOSABLE SYRINGE 1988-02-16
K003571 Terumo Medical Corp. SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE 2001-02-12
K812404 Nu Tech Medical Systems BUTTERFLY NEEDLE ASSEMBLY 1981-09-09

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0003-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04 Liberty Medical Supplies 2
Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024 Fresenius Medical Care Holdings, Inc. 2
10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003681915. Last updated year: 2026. Please use registration number 3003681915 when referencing this establishment in official correspondence.
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