Data / Medical devices / Netherlands / Iederz
Iederz: FDA-registered device maker in Groningen, Netherlands, 5 510(k) clearances
Iederz is registered with the FDA (registration 3015521867) in Groningen, Netherlands. It lists 1 device type. The FDA files 5 510(k) clearances under its listings, the newest dated September 15, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015521867
- Address
- Van der Hoopstraat 3, Groningen, Netherlands, 9716 JK
- Owner or operator
- iederz (10060588)
- Roles
- Repackager or relabeler
- First device listed
- May 29, 2019
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Unit, Cryosurgical, Accessories | GEH | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 15, 2016 | K161294 | Compound W Wart Removal System Dual Power | GEH | Substantially Equivalent | Medtech Products, Inc. | accessdata.fda.gov |
| August 14, 2015 | K151309 | Wartie Advanced Wart Remover or other proprietary name | GEH | Substantially Equivalent | Youmedical Corp BV | accessdata.fda.gov |
| June 12, 2014 | K140314 | WARTIE WART REMOVER | GEH | Substantially Equivalent | Yonmedical BV | accessdata.fda.gov |
| September 10, 2003 | K032271 | WARTNER WART REMOVAL SYSTEM, MODEL 66715 82000 (PRODUCT CODE NUMBER 52E022) | GEH | Substantially Equivalent | Wartner USA B.V. | accessdata.fda.gov |
| February 20, 2002 | K011708 | MODIFICATION TO WARTNER WART REMOVAL SYSTEM | GEH | Substantially Equivalent | Wartner Medical Products | accessdata.fda.gov |
Compare with other makers
Updated September 15, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.