FDA applicant
Consolidated Products & Services, Inc.
FDA records 7 decisions for Consolidated Products & Services, Inc. (North Quincy, MA) from 1989 to 1997: 7 510(k) clearances. Most are in product codes IMD (Pack, Hot Or Cold, Disposable) and KNX (Collector, Urine, (And Accessories) For…). Its devices cite 1 predicate, 1 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Consolidated Products & Services, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Consolidated Products & Services, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Consolidated Products & Services, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Consolidated”
FDA records each applicant name separately; these may or may not be the same firm.