FDA applicant
Rhealm Pharmaceuticals, Inc.
FDA records 1 decision for Rhealm Pharmaceuticals, Inc. (Delray Beach, FL) in 2000: 1 510(k) clearance. All are in product code MLY (Vapocoolant Device). 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 Rhealm Pharmaceuticals, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Rhealm Pharmaceuticals, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Rhealm Pharmaceuticals, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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