Medtronic Puerto Rico Operations Co., Villalba
Villalba, PR, US
MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA appears in FDA device records in Villalba, PR. 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 |
|---|---|---|---|---|---|
| 2649622 | 2649622 | MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA | RD. 149, KM. 56.3, Villalba, PR 00766 US | 2026 | and 26 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- LPBCardiac Ablation Percutaneous Catheter
- DRFCatheter, Electrode Recording, Or Probe, Electrode Recording
- DYGCatheter, Flow Directed
- DQYCatheter, Percutaneous
- OAECatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
- SGSDeep Brain Stimulation For The Treatment Of Dystonia
- OLMDeep Brain Stimulator For Obsessive Compulsive Disorder (Ocd)
- OJXDrug Eluting Permanent Left Ventricular (Lv) Pacemaker Electrode
- NVNDrug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- LWSImplantable Cardioverter Defibrillator (Non-Crt)
- DXYImplantable Pacemaker Pulse-Generator
- LWPImplantable Pulse Generator, Pacemaker (Non-Crt)
- QONImplanted Electrical Device Intended For Treatment Of Fecal Incontinence
- MRUImplanted Subcortical Electrical Stimulator (Motor Disorders)
- DWSInstruments, Surgical, Cardiovascular
- LNQIntestinal Stimulator
- DTDPacemaker Lead Adaptor
- OSRPacemaker/Icd/Crt Non-Implanted Components
- NVYPermanent Defibrillator Electrodes
- DTBPermanent Pacemaker Electrode
- KRGProgrammer, Pacemaker
- NKEPulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
- NVZPulse Generator, Permanent, Implantable
- MFRStimulator, Brain, Implanted, For Behavior Modification
- EZWStimulator, Electrical, Implantable, For Incontinence
- PJSStimulator, Electrical, Implanted, For Essential Tremor
- NHLStimulator, Electrical, Implanted, For Parkinsonian Symptoms
- MHYStimulator, Electrical, Implanted, For Parkinsonian Tremor
- GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)
- GZBStimulator, Spinal-Cord, Implanted (Pain Relief)
- LGWStimulator, Spinal-Cord, Totally Implanted For Pain Relief
- QRBStimulator, Spinal-Cord, Totally Implanted For Relief Of Pain Due To Diabetic Neuropathy
- MBXStimulator, Thalamic, Epilepsy, Implanted
- DRBStylet, Catheter
- DTFTools, Pacemaker Service
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain