Complexus Medical
Mishawaka, IN, US
Complexus Medical appears in FDA device records in Mishawaka, 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 |
|---|---|---|---|---|---|
| 3009887475 | 3009887475 | Complexus Medical | 55980 Russell Industrial Pkwy, Mishawaka, IN 46545 US | 2026 | and 46 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KTTAppliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- KWPAppliance, Fixation, Spinal Interlaminal
- KWQAppliance, Fixation, Spinal Intervertebral Body
- HWJAwl
- HXWBender
- HTQBroach
- KTZCaliper
- HXDClamp
- JDODevice, Fixation, Proximal Femoral, Implant
- IQODevice, Prosthesis Alignment
- MQNExternal Mandibular Fixator And/Or Distractor
- HWBExtractor
- HTJGauge, Depth
- EILGauge, Depth, Instrument, Dental
- FZXGuide, Surgical, Instrument
- FZYHammer, Surgical
- EJBHandle, Instrument, Dental
- HWAImpactor
- HXPInstrument, Bending Or Contouring
- HTZInstrument, Cutting, Orthopedic
- MDMInstrument, Manual, Surgical, General Use
- 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
- LXHOrthopedic Manual Surgical Instrument
- OLOOrthopedic Stereotaxic Instrument
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- HWMOsteotome
- OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- HRSPlate, Fixation, Bone
- NKGPosterior Cervical Screw System
- HXBProbe
- HSNProsthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
- JDCProsthesis, Elbow, Constrained, Cemented
- HSXProsthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer
- MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
- OIYProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
- JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
- HSDProsthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented
- KWTProsthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
- KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
- MBFProsthesis, Shoulder, Semi-Constrained, Metal/Polymer, Uncemented
- GADRetractor
- HXXScrewdriver
- PHXShoulder Prosthesis, Reverse Configuration
- MQPSpinal Vertebral Body Replacement Device
- PLRSpinal Vertebral Body Replacement Device - Cervical
- HWTTemplate
- NKBThoracolumbosacral Pedicle Screw System
- LRPTray, Surgical
- FSMTray, Surgical, Instrument
- KTETrocar, Ent
- HXCWrench
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.
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Data as of , FDA export datePage updated Source: openFDA, public domain