Abeon Medical Corporation
Abeon Medical Corporation holds FDA 510(k) medical device clearances, cleared in 2014, with 3 FDA device recalls on record.
Top product codes for Abeon Medical Corporation
FDA recalls by Abeon Medical Corporation
- Z-0686-2016 — Wilson Penile Implantation System Retractor Frame, Retractor Stays & Penile Elevation Strap, SINGLE USE ONLY Rx ONLY. Indicated to aid in tissue retraction during a surgical procedure.
- Z-0685-2016 — TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Indicated to aid in tissue retraction during a surgical procedure.
- Z-0684-2016 — TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY. Indicated for use in the retraction of soft tissue away from the operative surface.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Abeon Medical Corporation
Data sourced from openFDA. This site is unofficial and independent of the FDA.