FDA applicant
Pain Prevention Laboratory, Inc.
FDA records 1 decision for Pain Prevention Laboratory, Inc. (Northbrook, IL) in 1987: 1 510(k) clearance. All are in product code LWM (Device, Electrical Dental Anesthesia). 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 Pain Prevention Laboratory, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Pain Prevention Laboratory, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Pain Prevention Laboratory, 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 “Pain”
FDA records each applicant name separately; these may or may not be the same firm.