Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016248656

FEI Number

3016248656

Entity Name

POSEIDON MEDICAL INC.

City/State/Country

Pembroke Pines, FL, US

Establishment Address

1125 NW 132nd Avenue, Pembroke Pines, FL 33028, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Poseidon Medical Inc. (Owner Number: 10062215)

Owner / Operator Contact Address

1125 NW 132nd Avenue, Pembroke Pines, FL 33028, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P150039

All Registered Proprietary Names

Tryton Side Branch Stent

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MAF	Stent, Coronary	Unknown	Class 3	N/A	2019-12-30

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Poseidon Medical Inc.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
3004091615	Abbott Vascular Netherlands	Heerlen Limburg, NL
9681260	Boston Scientific Limited	GALWAY, IE
3011574793	CORTRONIK GmbH	Rostock-Warnemuende Mecklenburg-Western Pomerania, DE
3005111382	Boston Scientific International BV, European Dist. Ctr.	KERKRADE Limburg, NL
2024168	ABBOTT VASCULAR	Temecula, CA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016248656. Last updated year: 2026. Please use registration number 3016248656 when referencing this establishment in official correspondence.