Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009341014

FEI Number

3009341014

Entity Name

CINOVA MEDICAL INC.

City/State/Country

Phoenix, AZ, US

Establishment Address

3301 W Vernon Ave, Phoenix, AZ 85009, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Cinova Medical Inc. (Owner Number: 10047082)

Owner / Operator Contact Address

3301 W. Vernon Ave., Phoenix, AZ 85009, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

STRYKER Y-NEEDLE, 300 STRYKER LITEE Y-NEEDLE,100 STRYKER Y-NEEDLE,200 STRYKER Y-NEEDLE,400

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GDF	Guide, Needle, Surgical	General, Plastic Surgery	Class 1	878.4800	2014-06-25

Official Correspondent

Jose Castro

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Cinova Medical Inc.

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009341014. Last updated year: 2026. Please use registration number 3009341014 when referencing this establishment in official correspondence.