Ferry Machine Corporation
Little Ferry, NJ, US
FERRY MACHINE CORPORATION appears in FDA device records in Little Ferry, NJ. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. 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
- 2
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 |
|---|---|---|---|---|---|
| 3043543260 | 3043543260 | FERRY MACHINE CORPORATION | 112 Bauer Dr, Oakland, NJ 07436 US | 2026 | and 38 more, listed in full below |
| 3009959868 | 3009959868 | Ferry Machine Corporation | 75 Industrial Avenue, Little Ferry, NJ 07643 US | 2026 | and 38 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KWPAppliance, Fixation, Spinal Interlaminal
- KWQAppliance, Fixation, Spinal Intervertebral Body
- PMLBone Cement, Posterior Screw Augmentation
- OWIBone Fixation Cerclage, Sublaminar
- BSKCuff, Tracheal Tube, Inflatable
- DSIDetector And Alarm, Arrhythmia
- JDODevice, Fixation, Proximal Femoral, Implant
- IKNElectromyograph, Diagnostic
- OQGHip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
- OQIHip, Semi-Constrained, Cemented, Metal/Ceramic/Polymer + Additive, Porous Uncemented
- OQHHip, Semi-Constrained, Cemented, Metal/Polymer + Additive, Cemented
- DWSInstruments, Surgical, Cardiovascular
- ODPIntervertebral Fusion Device With Bone Graft, Cervical
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- PHMIntervertebral Fusion Device With Bone Graft, Thoracic
- OVEIntervertebral Fusion Device With Integrated Fixation, Cervical
- OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar
- MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- JDSNail, Fixation, Bone
- HAWNeurological Stereotaxic Instrument
- PDQNeurosurgical Nerve Locator
- LXHOrthopedic Manual Surgical Instrument
- OLOOrthopedic Stereotaxic Instrument
- MNIOrthosis, Spinal Pedicle Fixation
- NQWOrthosis, Spine, Plate, Laminoplasty, Metal
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- HWMOsteotome
- OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- HRSPlate, Fixation, Bone
- NKGPosterior Cervical Screw System
- MAYProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Cemented, Osteophilic Finish
- KWIProsthesis, Elbow, Hemi-, Radial, Polymer
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- JDIProsthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- LWJProsthesis, Hip, Semi-Constrained, Metal/Polymer, Uncemented
- MBLProsthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
- HSBRod, Fixation, Intramedullary And Accessories
- OURSacroiliac Joint Fixation
- HWCScrew, Fixation, Bone
- HXXScrewdriver
- MQPSpinal Vertebral Body Replacement Device
- KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories
- GWFStimulator, Electrical, Evoked Response
- ETNStimulator, Nerve
- FIPSubsystem, Water Purification
- NKBThoracolumbosacral Pedicle Screw System
- BTRTube, Tracheal (W/Wo Connector)
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