Pmbs, LLC

Pmbs, LLC holds 2 FDA 510(k) medical device clearances, first cleared 2015, most recent 2019, with 1 FDA device recall on record.

FDA recalls by Pmbs, LLC

Z-1266-2016 — The S.C.O.R.E.S. Unit (self contained operating room equipment sterilization unit)Class II·Terminated·2016-01-13

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 Pmbs, LLC

K190541 — MTS225 and MTS300 Multiple Tray Sterilization SystemsCode KCT·2019-11-05
K152014 — MTS300 Multiple Tray Sterilization SystemCode KCT·2015-10-20

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

Top product codes for Pmbs, LLC

FDA recalls by Pmbs, LLC

Recent clearances by Pmbs, LLC