Matrix Surgical Holdings, LLC/Matrix Surgical USA

Matrix Surgical Holdings, LLC/Matrix Surgical USA holds 2 FDA 510(k) medical device clearances, first cleared 2014, most recent 2018.

Top product codes for Matrix Surgical Holdings, LLC/Matrix Surgical USA

JEY — Dental1 device
KKY — General, Plastic Surgery1 device

Recent clearances by Matrix Surgical Holdings, LLC/Matrix Surgical USA

K180249 — OmniPore DUROMAX Surgical ImplantsCode JEY·2018-10-11
K133046 — OMNIPORE CUSTOMIZED SURGICAL IMPLANTSCode KKY·2014-05-14

Data sourced from openFDA. This site is unofficial and independent of the FDA.