Friedrich Daniels GmbH
SOLINGEN North Rhine-Westphalia, DE
FRIEDRICH DANIELS GMBH appears in FDA device records in SOLINGEN North Rhine-Westphalia, DE. 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 |
|---|---|---|---|---|---|
| 9611390 | 3002806773 | FRIEDRICH DANIELS GMBH | DOENHOFFSTRASSE 6, SOLINGEN North Rhine-Westphalia 42655 DE | 2026 | and 56 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
- HWJAwl
- HXWBender
- KTZCaliper
- HXDClamp
- FZSCurette, Surgical, General Use
- FZTCutter, Surgical
- HXZCutter, Wire
- GEGElevator, Surgical, General & Plastic Surgery
- HTPFile
- MQVFiller, Bone Void, Calcium Compound
- HTDForceps
- EMHForceps, Rongeur, Surgical
- GDHGouge, Surgical, General & Plastic Surgery
- FZXGuide, Surgical, Instrument
- OQGHip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented
- FHQHolder, Needle, Gastroenterologic
- HXPInstrument, Bending Or Contouring
- HWNInstrument, Compression
- HTZInstrument, Cutting, Orthopedic
- MDMInstrument, Manual, Surgical, General Use
- ODPIntervertebral Fusion Device With Bone Graft, Cervical
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- FSTLight, Surgical, Fiberoptic
- GFJMallet, Surgical, General & Plastic Surgery
- JDSNail, Fixation, Bone
- HAWNeurological Stereotaxic Instrument
- LXHOrthopedic Manual Surgical Instrument
- OLOOrthopedic Stereotaxic Instrument
- MNIOrthosis, Spinal Pedicle Fixation
- MNHOrthosis, Spondylolisthesis Spinal Fixation
- OSHPedicle Screw Spinal System, Adolescent Idiopathic Scoliosis
- HRSPlate, Fixation, Bone
- NKGPosterior Cervical Screw System
- HXBProbe
- KWIProsthesis, Elbow, Hemi-, Radial, Polymer
- LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
- MBLProsthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous
- KROProsthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer
- 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
- HWPPunch, Femoral Neck
- GACRasp, Surgical, General & Plastic Surgery
- HTOReamer
- GADRetractor
- HSBRod, Fixation, Intramedullary And Accessories
- HTXRongeur
- GDRSaw, Manual And Accessories
- LRWScissors, General, Surgical
- HWCScrew, Fixation, Bone
- HXXScrewdriver
- HWOSkid, Bone
- ETNStimulator, Nerve
- FMFSyringe, Piston
- FTYTape, Measuring, Rulers And Calipers
- HWTTemplate
- NKBThoracolumbosacral Pedicle Screw 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