Stockert GmbH
FREIBURG Baden-Wurttemberg, DE
STOCKERT GMBH appears in FDA device records in FREIBURG Baden-Wurttemberg, DE. FDA records list 5 510(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 5 510(k) clearances for Stockert GmbH between 2001 and 2007. The busiest year on record is 2007, with 2. The most recent is 2007, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2001 | 1 |
| 2005 | 1 |
| 2006 | 1 |
| 2007 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K070336 | STOCKERT NEURO N50, MODEL12267 | GXD | Substantially Equivalent | |
| K070134 | MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098 | BXN | Substantially Equivalent | |
| K061983 | STIMUPLEX PEN | BXN | Substantially Equivalent | |
| K052313 | STIMUPLEX HNS-12, MODEL 4892098 | BXN | Substantially Equivalent | |
| K003983 | STIMUPLEX HNS-11 | BXN | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3015537323 | 3015537323 | STOCKERT GMBH | BOETZINGER STRASSE 31, FREIBURG Baden-Wurttemberg 79111 DE | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- LPBCardiac Ablation Percutaneous Catheter
- DRFCatheter, Electrode Recording, Or Probe, Electrode Recording
- OAECatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
- OADCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
- GXDGenerator, Lesion, Radiofrequency
- BXNStimulator, Nerve, Battery-Powered
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.
Where there is a record, this is where it appears: what was checked, when it was checked, and the current status. An MDM Verified badge on another website links to a verify address on this domain that resolves to this section. A badge that does not resolve here is not ours.
MDM coverage
MDM coverage of this company lists here, newest first. Submit news.
Is this your company?
This page is built from public FDA records. Company pages are free and factual, and stay free whether or not anyone claims them. Membership never changes editorial coverage or vetting outcomes.
Claiming lets Stockert GmbH edit what it says about itself and list the categories it works in. It grants no badge: claiming is not verification.
Data as of , FDA export datePage updated Source: openFDA, public domain