POSEIDON MEDICAL TECHNOLOGY LLC

FDA Device Registration & Listing · San Dimas, CA, US · Registration 3042370483

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
3042370483
FEI Number
3042370483
Entity Name
POSEIDON MEDICAL TECHNOLOGY LLC
City/State/Country
San Dimas, CA, US
Establishment Address
1305 W Arrow Hwy Ste 206, San Dimas, CA 91773, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Poseidon Medical Technology LLC (Owner Number: 10094419)
Owner / Operator Contact Address
1305 W Arrow Highway, unit 206, San Dimas, CA 91773, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K211484
PMA Number
N/A

All Registered Proprietary Names

AnderMed Safety Closed IV Catheter for CT use AnderMed Disposable IV Catheter Safety AnderMed Safety Closed IV Catheter AnderMed Disposable IV Catheter Poseidon Medical Technology P-2 Wheelchair Poseidon Medical Technology P-1 Wheelchair Ande Healthcare Disposable Enteral Feeding Syringe AnderMed Disposable Enteral Syringe Disposable Enteral Feeding Syringe Poseidon Medical Technology Dressing Change Kit AnderMed Disposable Sterile Syringe with Safety Needle AnderMed Disposable Safety Needles Disposable Sterile Syringe AnderMed Disposable Sterile Syringe with Needle AnderMed Disposable Sterile Syringe

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days General Hospital Class 2 880.5200 2025-11-27
IOR Wheelchair, Mechanical Physical Medicine Class 1 890.3850 2025-11-28
PNR Enteral Syringes With Enteral Specific Connectors Gastroenterology, Urology Class 2 876.5980 2025-11-27
NAE Dressing, Wound, Hydrogel Without Drug And/Or Biologic General, Plastic Surgery Class 1 878.4022 2025-11-28
FMI Needle, Hypodermic, Single Lumen General Hospital Class 2 880.5570 2025-11-28
MEG Syringe, Antistick General Hospital Class 2 880.5860 2025-11-28
FMF Syringe, Piston General Hospital Class 2 880.5860 2025-11-28

Official Correspondent

YUZE JING

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Poseidon Medical Technology LLC
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
K943349 Quinton, Inc. MAHURKAR DUAL LUMEN CATHETER 1995-03-22
K912158 Medical Device Inspection Co., Inc. CENTRAL VENOUS CATHETER DRESSING CHANGE TRAY 1991-10-23
K935211 Brookefield Hunter, Inc. WALK N CHAIR 1994-02-02
K832685 Health America WHEELCHAIR-VARIOUS MODELS 1983-09-20
K203410 Shantou Wealy Medical Instrument Co.,Ltd ENFit Disposable Enteral Syringe 2021-06-28

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0002-2024 ARROW INTERNATIONAL Inc. 2
Arrow ErgoPack Complete, Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-42854- PCN1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Z-0003-2024 ARROW INTERNATIONAL Inc. 2
Arrow Pressure Injectable Arrowg+ard Blue Plus Four-Lumen CVC, REF CDC-45854-P1A; catheter, intravascular, therapeutic, long-term greater than 30 days
Z-0009-2023 B Braun Medical Inc 2
Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02. A passive anti-needle device to provide venous or arterial access.
Z-0025-2024 Becton Dickinson Infusion Therapy Systems Inc. 2
REF: 386862, BD Cathena Safety IV catheter with BD Multiguard Technology, 20 GA 1.00 IN, 1.1 x 25 mm 64 mL/min , Rx Only, Sterile EO
Z-0002-2022 Bard Peripheral Vascular Inc 2
REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042370483. Last updated year: 2026. Please use registration number 3042370483 when referencing this establishment in official correspondence.
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