Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011671735

FEI Number

3011671735

Entity Name

RAMKO INJECTION INC

City/State/Country

Hemet, CA, US

Establishment Address

3551 Tanya Ave, Hemet, CA 92545, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Ramko Injection Inc (Owner Number: 10080231)

Owner / Operator Contact Address

3551 Tanya Ave, Hemet, CA 92545, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GIO	Tube, Collection, Capillary Blood	Hematology	Class 1	864.6150	2021-01-20

Official Correspondent

Matthew Andrei

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ramko Injection 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 3011671735. Last updated year: 2026. Please use registration number 3011671735 when referencing this establishment in official correspondence.