FDA applicant
Tillotson Healthcare Corp.
FDA records 20 decisions for Tillotson Healthcare Corp. (Bedford, NH) from 1995 to 2002: 20 510(k) clearances. Most are in product codes LYY (Latex Patient Examination Glove) and LZA (Polymer Patient Examination Glove). Its devices cite 11 predicates, 7 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 Tillotson Healthcare Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Tillotson Healthcare Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Tillotson Healthcare Corp.’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 “Tillotson”
FDA records each applicant name separately; these may or may not be the same firm.