Meticuly Co., Ltd. is one of 32 FDA 510(k) medical device manufacturers from Thailand in the dataset, ranked by real submission volume.
Meticuly Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: METICULY Patient-specific titanium mesh implant, METICULY Patient-specific titanium maxillofacial mesh implant, Meticuly Patient-Specific Titanium Mesh Implant
4
Total
4
Cleared
0
Denied
Meticuly Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Muang Nonthaburi, TH.
Latest FDA clearance: Jul 2026. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Meticuly Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdr Solutions Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Meticuly Co., Ltd.
4 devices
Cleared
Jul 25, 2026
METICULY Patient-specific CMF solution
Dental
302d
Cleared
Jan 14, 2026
METICULY Patient-specific titanium mesh implant
Neurology
120d
Cleared
Apr 30, 2024
METICULY Patient-specific titanium maxillofacial mesh implant
Dental
225d
Cleared
Dec 21, 2021
Meticuly Patient-Specific Titanium Mesh Implant
Neurology
341d