Gebr. Brasseler GmbH & Co. KG
LEMGO North Rhine-Westphalia, DE
GEBR. BRASSELER GMBH & CO. KG appears in FDA device records in LEMGO North Rhine-Westphalia, DE. FDA records list 2 510(k) clearances between and , 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) clearance history
FDA records hold 2 510(k) clearances for Gebr. Brasseler GmbH & Co. KG between 2007 and 2013. The busiest year on record is 2007, with 1. The most recent is 2013, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2007 | 1 |
| 2013 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 8010468 | 3002806577 | GEBR. BRASSELER GMBH & CO. KG | ATTN.: Petra Meier, LEMGO North Rhine-Westphalia D-32657 DE | 2026 | and 40 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- NHAAbutment, Implant, Dental, Endosseous
- NDPAccessories, Implant, Dental, Endosseous
- KWQAppliance, Fixation, Spinal Intervertebral Body
- HTWBit, Drill
- GFABlade, Saw, General & Plastic Surgery, Surgical
- EJLBur, Dental
- GFFBur, Surgical, General & Plastic Surgery
- OHWBurr, Corneal, Battery Powered, Rust Ring Removal
- GWMDevice, Monitoring, Intracranial Pressure
- EHJDisk, Abrasive
- DZIDrill, Bone, Powered
- DZADrill, Dental, Intraoral
- HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)
- HWRDriver, Prosthesis
- GFCDriver, Surgical, Pin
- EKSFile, Pulp Canal, Endodontic
- FZXGuide, Surgical, Instrument
- EKMGutta-Percha
- EFBHandpiece, Air-Powered, Dental
- EKXHandpiece, Direct Drive, Ac-Powered
- DZEImplant, Endosseous, Root-Form
- DZPInstrument, Diamond, Dental
- EIYInstrument, Filling, Plastic, Dental
- HWEInstrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- LQYLocator, Root Apex
- SBFOrthopedic Augmented Reality
- LXHOrthopedic Manual Surgical Instrument
- OLOOrthopedic Stereotaxic Instrument
- HTYPin, Fixation, Smooth
- JDWPin, Fixation, Threaded
- JEYPlate, Bone
- HRSPlate, Fixation, Bone
- EKRPlugger, Root Canal, Endodontic
- EHLPoint, Abrasive
- EKNPoint, Paper, Endodontic
- ELRPost, Root Canal
- EKPReamer, Pulp Canal, Endodontic
- KIFResin, Root Canal Filling
- OURSacroiliac Joint Fixation
- ELCScaler, Ultrasonic
- HWCScrew, Fixation, Bone
- EKKSpreader, Pulp Canal Filling Material, Endodontic
- EHMStrip, Polishing Agent
- EICSyringe, Periodontic, Endodontic, Irrigating
- HWXTap, Bone
- HWTTemplate
- NKBThoracolumbosacral Pedicle Screw System
- FSMTray, Surgical, Instrument
- HXCWrench
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