Pmbs, LLC

Stockton, NJ, US

Pmbs, LLC appears in FDA device records in Stockton, NJ. FDA records list one 510(k) clearance, no PMA records and no registered establishments. As of 2026-09-10, FDA records show one recall for this company.

510(k) clearances: 1
PMA records: 0
Recall records: 1
Registered establishments: 0

510(k) clearance history

FDA records hold 1 510(k) clearance for Pmbs, LLC in 2015.

Clearances by year, as a table

510(k) clearance decisions for Pmbs, LLC, by decision year
Year	Clearances
2015	1

510(k) clearances on record, most recent first
K number	Device	Product code	Decision	Decision date
K152014	MTS300 Multiple Tray Sterilization System	KCT	Substantially Equivalent	2015-10-20

Registered establishments

No FDA establishment registrations recorded against this company.

FDA product codes

KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories

Recall records

This record is listed because FDA’s enforcement report for the recall names this company, while the recall record itself carries the recalling firm under another name.

Device recall records naming this company, most recent first
Recall	Product	Reason	Classification	Initiated	Status
Z-1266-2016	The S.C.O.R.E.S. Unit (self contained operating room equipment sterilization unit)	Water retention issues. Units with filters that remain wet after the sterilization may compromised sterility.	Class II	2016-01-13	Terminated

Verification record

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Data as of 2026-09-28, FDA export datePage updated 2026-09-05Source: openFDA, public domain