Nihon Kohden Tomioka Production Center
TOMIOKA-SHI Gunma, JP
NIHON KOHDEN TOMIOKA PRODUCTION CENTER appears in FDA device records in TOMIOKA-SHI Gunma, JP. FDA records list no 510(k) clearances, no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
- 510(k) clearances
- 0
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 1
510(k) clearance history
No 510(k) clearance records for this company in the ingested FDA data.
No 510(k) clearance records in the ingested FDA data.
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 8030229 | 3002807739 | NIHON KOHDEN TOMIOKA PRODUCTION CENTER | 1-1 Tajino, TOMIOKA-SHI Gunma 370-2314 JP | 2026 | and 17 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- OMAAmplitude-Integrated Electroencephalograph
- CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- OMBAutomatic Event Detection Software For Full-Montage Electroencephalograph
- ORTBurst Suppression Detection Software For Electroencephalograph
- BZAConnector, Airway (Extension)
- DSIDetector And Alarm, Arrhythmia
- GZODevice, Galvanic Skin Response Measurement
- JXEDevice, Nerve Conduction Velocity Measurement
- DPSElectrocardiograph
- GYCElectrode, Cortical
- GXYElectrode, Cutaneous
- IKNElectromyograph, Diagnostic
- MNKEndoscopic Bite Block
- GWQFull-Montage Standard Electroencephalograph
- GYBMedia, Electroconductive
- OUGMedical Device Data System
- DRTMonitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- MHXMonitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
- OLTNon-Normalizing Quantitative Electroencephalograph Software
- OMCReduced- Montage Standard Electroencephalograph
- OLVStandard Polysomnograph With Electroencephalograph
- GWJStimulator, Auditory, Evoked Response
- GWFStimulator, Electrical, Evoked Response
- KOIStimulator, Nerve, Peripheral, Electric
- GWEStimulator, Photic, Evoked Response
- DRGTransmitters And Receivers, Physiological Signal, Radiofrequency
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Nihon Kohden Tomioka Production Center edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain