Ahip Internal Trigger Point Wand Model: 1

DEN100023 is the FDA 510(k) clearance record for AHIP INTERNAL TRIGGER POINT WAND MODEL: 1, a class II device, cleared for National Center For Pelvic Pain Research Devices, on 2012-11-20 under FDA product code OSD (Massager, Therapeutic, To Internally Massage Trigger Points In The Pelvic Floor Musculature). FDA's definition for product code OSD reads: "Rectal or vaginal use manual therapeutic massager device to massage irritable, sore trigger points (trps) in the pelvic floor musculature in order to reduce internal pelvic floor trigger point sensitivity". FDA records list one 510(k) clearance for National Center For Pelvic Pain Research Devices,. As of 2026-09-10, FDA records show no recalls naming DEN100023.