Ackermann Instrumente GmbH
RIETHEIM, WEILHEIM Baden-Wurttemberg, DE
ACKERMANN INSTRUMENTE GMBH appears in FDA device records in RIETHEIM, WEILHEIM Baden-Wurttemberg, DE. FDA records list 3 510(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 3 510(k) clearances for Ackermann Instrumente GmbH between 1998 and 2015. The busiest year on record is 1998, with 1. The most recent is 2015, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1998 | 1 |
| 2011 | 1 |
| 2015 | 1 |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 8010273 | 4486 | ACKERMANN INSTRUMENTE GMBH | EISENBAHNSTR. 65-67, RIETHEIM, WEILHEIM Baden-Wurttemberg D-78604 DE | 2026 | and 48 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- NBHAccessories, Arthroscopic
- GCXApparatus, Suction, Operating-Room, Wall Vacuum Powered
- HBTApplier, Hemostatic Clip
- GDOApplier, Surgical, Clip
- EOQBronchoscope (Flexible Or Rigid)
- KTZCaliper
- FWFCamera, Television, Endoscopic, Without Audio
- FGYCannula, Injection
- GEACannula, Surgical, General & Plastic Surgery
- KCECannulae, Bronchial
- GDJClamp, Surgical, General & Plastic Surgery
- FLGCleaner, Ultrasonic, Medical Instrument
- MCHClip, Hemostatic
- FZPClip, Implantable
- KAPCurette, Nasal
- FZSCurette, Surgical, General Use
- FGODislodger, Stone, Flexible
- GDIDissector, Surgical, General & Plastic Surgery
- KBMDissector, Tonsil
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- GENForceps, General & Plastic Surgery
- GDFGuide, Needle, Surgical
- GDZHandle, Scalpel
- LGGInstrument, Cast Application/Removal, Manual
- HTZInstrument, Cutting, Orthopedic
- MDMInstrument, Manual, Surgical, General Use
- GZXInstrument, Microsurgical
- KDCInstrument, Surgical, Disposable
- DWSInstruments, Surgical, Cardiovascular
- HIFInsufflator, Laparoscopic
- ODPIntervertebral Fusion Device With Bone Graft, Cervical
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- KDDKit, Surgical Instrument, Disposable
- KTGKnife, Ent
- EMFKnife, Surgical
- GCJLaparoscope, General & Plastic Surgery
- NTNLed Light Source
- OUGMedical Device Data System
- FTXMirror, General & Plastic Surgery
- ERAOtoscope
- HXBProbe
- KAWPunch, Antrum
- KTFPunch, Ent
- KAYPunch, Nasal
- LRYPunch, Surgical
- HTRRasp
- GADRetractor
- FFORetractor, Self-Retaining
- LRWScissors, General, Surgical
- JOKScissors, Medical, Disposable
- EPYSpeculum, Ent
- FXESpeculum, Non-Illuminated
- HDFSpeculum, Vaginal, Metal
- CCXSupport, Patient Position
- BWNTable And Attachments, Operating-Room
- FSMTray, Surgical, Instrument
- KCBTube, Tonsil Suction
- EZOUrethrotome
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
