Avalign Delivery Systems Division
Greenwood, IN, US
Avalign Delivery Systems Division appears in FDA device records in Greenwood, IN. 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 |
|---|---|---|---|---|---|
| 1835444 | 3000717687 | Avalign Delivery Systems Division | 2121 SOUTHTECH DRIVE, Greenwood, IN 46143 US | 2026 | and 32 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- NBHAccessories, Arthroscopic
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KWPAppliance, Fixation, Spinal Interlaminal
- KWQAppliance, Fixation, Spinal Intervertebral Body
- HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)
- MBIFastener, Fixation, Nondegradable, Soft Tissue
- HCFInstrument, Ligature Passing And Knot Tying
- MDMInstrument, Manual, Surgical, General Use
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar
- QLRManual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices
- LXHOrthopedic Manual Surgical Instrument
- OLOOrthopedic Stereotaxic Instrument
- OJHOrthopedic Tray
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- 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
- NTGProsthesis, Ankle, Uncemented, Non-Constrained
- LZOProsthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- MEHProsthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate
- MBLProsthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
- MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- KWTProsthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
- PAOProsthesis, Shoulder, Semi-Constrained, Metal/Polymer + Additive, Cemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- MBFProsthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
- GZTRetractor, Self-Retaining, For Neurosurgery
- HSBRod, Fixation, Intramedullary And Accessories
- HWCScrew, Fixation, Bone
- PHXShoulder Prosthesis, Reverse Configuration
- MQPSpinal Vertebral Body Replacement Device
- KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories
- ETNStimulator, Nerve
- HWTTemplate
- NKBThoracolumbosacral Pedicle Screw System
- LRPTray, Surgical
- FSMTray, Surgical, Instrument
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