Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010667677

FEI Number

3010667677

Entity Name

DVL-OP MEDICO INC

City/State/Country

Valencia, CA, US

Establishment Address

29021 Avenue Penn, Valencia, CA 91355, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

DVL-op MEDICO Inc (Owner Number: 10046315)

Owner / Operator Contact Address

29021 Ave Penn, Valencia, CA 91355, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GP4000 Greenpulse Hip Set Standard FL1611 Greenpulse SZ Washing Plug FL1014 Greenpulse Airhose FL1015 Greenpulse Airhose MA7 connector GP4101 Greenpulse Hip Set Suction FL1601 Greenpulse Zimmer Washing Plug FL1602 Greenpulse AO Washing Plug GP4001 Greenpulse Knee Set Standard GP2010 Greenpulse Handpiece AO connector FL1016 Greenpulse Airhose AGA Instrument Air connector OLAC2115 OrthoLavage AC Power Supply 115 Volt. GP4100 Greenpulse Hip Set Suction GP2000 Greenpulse Handpiece Zimmer connector OL1100 OrthoLavage® Hip/Knee Set GP4200 Greenpulse Soft Tissue Set OLAC2230 OrthoLavage AC Power Supply 230 Volt. OL1200 OrthoLavage Soft tissue Set Motiva® Channel Separator

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FQH	Lavage, Jet	General Hospital	Class 2	880.5475	2014-03-05
GDI	Dissector, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2025-06-01

Official Correspondent

Magda Forsberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DVL-op MEDICO Inc

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
K213616	Becton, Dickinson and Company	BD Surgiphor Antimicrobial Irrigation System	2022-03-23

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010667677. Last updated year: 2026. Please use registration number 3010667677 when referencing this establishment in official correspondence.