FDA applicant
Reliefband Technologies, LLC
FDA records 3 decisions for Reliefband Technologies, LLC (Horsham, PA) from 2017 to 2019: 3 510(k) clearances. All are in product code GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Since 2016 its 510(k)s took a median of 79 days from receipt to decision, against 156 for FDA’s reviews in the same codes and years. Its devices cite 3 predicates, 3 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Reliefband Technologies”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Reliefband Technologies, LLC’s devices, and how often a recall has named them.
FDA decisions per year
2in 2019
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Reliefband Technologies, LLC’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) Report