Skip to the page

Data / Medical devices / Germany / Polymedics Innovations

Polymedics Innovations: FDA-registered device maker in Kirchheim unter Teck Baden-Wurttemberg, Germany, 2 510(k) clearances

Polymedics Innovations is registered with the FDA (registration 3007710611) in Kirchheim unter Teck Baden-Wurttemberg, Germany. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 28, 2017. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3007710611
Address
Am Hegelesberg 1, Kirchheim unter Teck Baden-Wurttemberg, Germany, 73230
Owner or operator
Polymedics Innovations (10029744)
Roles
Manufacturer
First device listed
June 22, 2009
Registered through
2026
Brand names listed
SupraSDRM, Suprathel CW, Suprathel Hand, Suprathel Wound and Burn Dressing

Devices it lists

DeviceProduct codeClassRoleSource
Absorbable Synthetic Wound DressingQSZUManufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 28, 2017K170213SupraSDRM Biodegradable Matrix Wound DressingQSZSubstantially EquivalentPolymedics Innovations, GmbHaccessdata.fda.gov
May 20, 2009K090160SUPRATHEL WOUND AND BURN DRESSINGQSZSubstantially EquivalentPolymedics Innovations, GmbHaccessdata.fda.gov

Compare with other makers

Updated June 28, 2017. 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.