Hathor Professional Skincare , Ltd. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Hathor Professional Skincare , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Sutil Rich Personal Lubricant, Sutil Luxe Personal Lubricant (models 1126, 0009, 0010, 0011)
3
Total
3
Cleared
0
Denied
Hathor Professional Skincare , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Victoria, CA.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Hathor Professional Skincare , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hathor Professional Skincare , Ltd.
3 devices
Cleared
Jun 09, 2026
Sutil Pure Personal Lubricant (models 1148, 1145, 1146, 1147)
Obstetrics & Gynecology
270d
Cleared
May 02, 2025
Sutil Rich Personal Lubricant
Obstetrics & Gynecology
60d
Cleared
Jan 21, 2025
Sutil Luxe Personal Lubricant (models 1126, 0009, 0010, 0011)
Obstetrics & Gynecology
244d