Banyan Medical, LLC
Banyan Medical, LLC holds FDA 510(k) medical device clearance, cleared in 2014, with 2 FDA device recalls on record.
Top product codes for Banyan Medical, LLC
FDA recalls by Banyan Medical, LLC
- Z-0075-2017 — Banyan Medical 5 x 55mm Pyramidal Tip Trocar w/ 2X Cannula w/ Sideport. Laproscopic Use- Sterile Single Use Only Product Code 400-009
- Z-0074-2017 — Banyan Medical 5 x 55mm Regular Pyramidal Trocar and 2x Cannula. For Laproscopic Use- Sterile Single Use Only. Product Code 400-008
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 Banyan Medical, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.