INNOKAS MEDICAL OY

FDA Device Registration & Listing · KEMPELE Pohjois-Pohjanmaa, FI · Registration 3007615597

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3007615597
FEI Number
3007615597
Entity Name
INNOKAS MEDICAL OY
City/State/Country
KEMPELE Pohjois-Pohjanmaa, FI
Establishment Address
Vihikari 10, KEMPELE Pohjois-Pohjanmaa 90440, FI
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Innokas Yhtyma Oy (Owner Number: 10026175)
Owner / Operator Contact Address
Vihikari 10, KEMPELE, FI-14 90440, FI
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PhysioTouch LymphaTouch VC150 CYPRA HIT1, HIT3 HIT5, HIT6, HITM, HITSD, SMARTPHANTOM CT, SMARTPHANTOM RT, STATICPHANTOM Keikku Catalyst+; Catalyst+ HD; Catalyst+ HD Ring Gantry; Catalyst+ PT; Catalyst+ PT X4 Sentinel 4DCT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ISA Massager, Therapeutic, Electric Physical Medicine Class 1 890.5660 2011-08-17
MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms) Cardiovascular Class 2 870.2300 2014-11-11
IWE Monitor, Patient Position, Light-Beam Radiology Class 1 892.5780 2020-11-20
DQD Stethoscope, Electronic Cardiovascular Class 2 870.1875 2025-12-12
IYE Accelerator, Linear, Medical Radiology Class 2 892.5050 2020-11-20
IYE Accelerator, Linear, Medical Radiology Class 2 892.5050 2023-09-29

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Innokas Yhtyma Oy
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3010399798 Innokas Medical Estonia Ou Tallinn Harjumaa, EE

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K071802 Mammendorfer Institut Fur Physik Und Medizin GmbH TESLA GUARD, MODEL EFT G04 2007-11-09
K124061 Invivo Corporation MRI PATIENT MONITORING SYSTEM (MODEL 865214) 2013-02-22
K101264 Remote Diagnostic Technologies , Ltd. TEMPUS IC PROFESSIONAL PATIENT MONITOR 2010-05-11
K113105 Remote Diagnostic Technologies , Ltd. TEMPUSIC PATIENT MONITOR 2011-12-15
K134014 Remote Diagnostic Technologies , Ltd. TEMPUS PRO ACCESSORIES (ULTRASOUND & VIDEO LARYNGOSCOPE PROBE) 2014-08-12

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2015 Invivo Corporation 2
Philips Expression MR200 MRI Patient Monitoring System Model 866120
Z-0004-2023 Philips North America Llc 2
MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.
Z-0011-04 GE Medical Systems Information Technologies 2
Power cord manufactured by ElectriCord Manufacturing Company , P/N 316579, used with DINAMAP Patient Monitors as Follows: DINAMAP PRO Series, DINAMAP PRO 1000 Monitor under both the Critikon and GE Medical Systems. The company name EliectriCord is on the power cord plug.
Z-0042-2015 Mckesson Information Solutions LLC 2
McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
Z-2183-2011 Remote Diagnostic Technologies Ltd. The Old Coach House, The Av. Farleigh Wallop, Basingstoke Hampshire United Kingdom 2
TEMPUS IC PROFESSIONAL Patient Monitor, Part No. 00-1002, Manufactured by: Remote Diagnostics Technologies Ltd., The Old Coach House, Farleigh Wallop, Hants, UK RG25 2HT. Indicated for 3 Lead ECG monitoring and 12 Lead ECG recording, non-invasive blood pressure (NIBP), respiration, end-tidal C02 (ETCO 2), pulse oximetry (SP02) and tympanic temperature.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007615597. Last updated year: 2026. Please use registration number 3007615597 when referencing this establishment in official correspondence.
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