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Poseidon Medical Technology LLC: FDA-registered device maker in San Dimas, CA, United States, 4 510(k) clearances

Name: Poseidon Medical Technology LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Poseidon Medical Technology LLC is registered with the FDA (registration 3042370483) in San Dimas, CA, United States. It lists 7 device types. The FDA files 4 510(k) clearances under its listings, the newest dated March 1, 2022. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3042370483
Address: 1305 W Arrow Hwy Ste 206, San Dimas, CA, United States, 91773
Owner or operator: Poseidon Medical Technology LLC (10094419)
Roles: Complaint file establishment
First device listed: November 27, 2025
Registered through: 2026
Brand names listed: Ande Healthcare Disposable Enteral Feeding Syringe, AnderMed Disposable Enteral Syringe, AnderMed Disposable IV Catheter, AnderMed Disposable IV Catheter Safety, AnderMed Disposable Safety Needles, AnderMed Disposable Sterile Syringe, AnderMed Disposable Sterile Syringe with Needle, AnderMed Disposable Sterile Syringe with Safety Needle and more

Devices it lists

Device	Product code	Class	Role	Source
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	FOZ	2	Complaint file establishment	accessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or Biologic	NAE	1	Complaint file establishment	accessdata.fda.gov
Enteral Syringes With Enteral Specific Connectors	PNR	2	Complaint file establishment	accessdata.fda.gov
Needle, Hypodermic, Single Lumen	FMI	2	Complaint file establishment	accessdata.fda.gov
Syringe, Antistick	MEG	2	Complaint file establishment	accessdata.fda.gov
Syringe, Piston	FMF	2	Complaint file establishment	accessdata.fda.gov
Wheelchair, Mechanical	IOR	1	Complaint file establishment	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 1, 2022	K211484	Disposable Sterile Syringe with Safety Needle; Disposable Sterile Syringe with Needle; Disposable Sterile Syringe; Disposable Safety Needles	MEG	Substantially Equivalent	Shinva Ande Healthcare Apparatus Co., Ltd.	accessdata.fda.gov
July 23, 2021	K202060	Disposable IV catheter	FOZ	Substantially Equivalent	Shinva Ande Healthcare Apparatus Co., Ltd.	accessdata.fda.gov
September 12, 2020	K193657	Disposable Enteral Feeding Syringe with Enfit Connector	PNR	Substantially Equivalent	Shinva Ande Healthcare Apparatus Co., Ltd.	accessdata.fda.gov
October 5, 2005	K052468	YK9000 SERIES MANUAL WHEELCHAIR	IOR	Substantially Equivalent	Intco Metal Products (Zhenjiang) Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated March 1, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.