Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005536872

FEI Number

3005536872

Entity Name

INNOVATIVE INNOVATIONS INC.

City/State/Country

Henderson, NV, US

Establishment Address

1132 Santa Ynez Ave., Henderson, NV 89002, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

INNOVATIVE INNOVATIO (Owner Number: 9081220)

Owner / Operator Contact Address

1132 Santa Ynez Ave, Henderson, NV 89002, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K041694

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
KAD	Elevator, Ent	Ear, Nose, Throat	Class 1	874.4420	2008-09-14
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2007-04-17
DXN	System, Measurement, Blood-Pressure, Non-Invasive	Cardiovascular	Class 2	870.1130	2007-10-22
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2008-09-14
HLJ	Ophthalmoscope, Battery-Powered	Ophthalmic	Class 2	886.1570	2017-12-21
EPY	Speculum, Ent	General, Plastic Surgery	Class 1	878.1800	2008-09-14
KAQ	Gouge, Nasal, Ent	Ear, Nose, Throat	Class 1	874.4420	2008-09-14
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2007-10-22
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2008-09-14
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2007-10-22

Official Correspondent

James (jim) SCHMITZ

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INNOVATIVE INNOVATIO

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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08
K100940	Andon Health Co, Ltd.	FULLY AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR, MODEL KD-5965	2010-06-29
K251581	Shenzhen Hingmed Medical Instrument Co., Ltd.	Wearable Ambulatory Blood Pressure Monitor (WBP-02A)	2026-02-13
K200521	Health & Life Co., Ltd.	Full Automatic(NIBP) Blood Pressure Monitor	2020-06-12
K152003	Andon Health Co, Ltd.	iHealth BP3L Wireless Blood Pressure Monitor	2015-09-24

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0032-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001
Z-0033-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.
Z-0034-2025	MEDLINE INDUSTRIES, LP Northfield	2	MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only

Similar Registrations

Registration Number	Establishment Name	Location
3003435550	HAFNER CHIRURGISCHE INSTRUMENTE	BALGHEIM Baden-Wurttemberg, DE
8010155	A.HANDTE MEDIZINTECHNIK GMBH & CO. KG	TUTTLINGEN Baden-Wurttemberg, DE
3043355002	PILOTIS TECH LLC	Brookhaven, GA, US
3014967149	GLW, Inc.	Englewood Cliffs, NJ, US
3014334038	Integra LifeSciences Production Corporation	Mansfield, MA, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005536872. Last updated year: 2026. Please use registration number 3005536872 when referencing this establishment in official correspondence.