BK210661 - RegenKit-Wound Gel-2
510(k) Number: BK210661
Applicant: RegenLab SA
Device Name: RegenKit®-Wound Gel-2
Decision Date: 7/8/2022
On Oct. 1, 2024, the FDA began implementing a reorganization impacting many parts of the agency. We are in the process of updating FDA.gov content to reflect these changes.
510(k) Number: BK210661
Applicant: RegenLab SA
Device Name: RegenKit®-Wound Gel-2
Decision Date: 7/8/2022