Flex-Cell Precision, Inc.
Lancaster, PA, US
FLEX-CELL PRECISION, INC. appears in FDA device records in Lancaster, PA. 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 |
|---|---|---|---|---|---|
| 3010120135 | 3010120135 | FLEX-CELL PRECISION, INC. | 1151 S Duke St, Lancaster, PA 17602 US | 2026 | and 29 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
- OWIBone Fixation Cerclage, Sublaminar
- DSIDetector And Alarm, Arrhythmia
- JDODevice, Fixation, Proximal Femoral, Implant
- 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
- ODPIntervertebral Fusion Device With Bone Graft, Cervical
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- OVEIntervertebral Fusion Device With Integrated Fixation, Cervical
- OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar
- MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
- HAWNeurological Stereotaxic Instrument
- OLOOrthopedic Stereotaxic Instrument
- MNIOrthosis, Spinal Pedicle Fixation
- NQWOrthosis, Spine, Plate, Laminoplasty, Metal
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- HRSPlate, Fixation, Bone
- NKGPosterior Cervical Screw System
- NQPPosterior Metal/Polymer Spinal System, Fusion
- 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
- MJOProsthesis, Intervertebral Disc
- OURSacroiliac Joint Fixation
- HWCScrew, Fixation, Bone
- MQPSpinal Vertebral Body Replacement Device
- PEKSpinous Process Plate
- KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories
- ETNStimulator, Nerve
- FIPSubsystem, Water Purification
- NKBThoracolumbosacral Pedicle Screw System
- QHPVertebral Body Tethering System
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