Data / Medical devices / Thailand / Meticuly Co., Ltd.
Meticuly Co., Ltd.: FDA-registered device maker in Bangkok Krung Thep Maha Nakhon, Thailand, 4 510(k) clearances
Meticuly Co., Ltd. is registered with the FDA (registration 3027157194) in Bangkok Krung Thep Maha Nakhon, Thailand. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated July 25, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3027157194
- Address
- Soi Chula 7, Wang Mai, Pathum Wan 924 B bldg., Rm. B116-118, B210-212, Bangkok Krung Thep Maha Nakhon, Thailand, 10330
- Owner or operator
- Meticuly Co., Ltd. (10087798)
- Roles
- Manufacturer
- First device listed
- April 11, 2023
- Registered through
- 2026
- Brand names listed
- METICULY Patient-specific titanium maxillofacial mesh implant, METICULY Patient-specific titanium mesh implant
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Plate, Bone | JEY | 2 | Manufacturer | accessdata.fda.gov |
| Plate, Cranioplasty, Preformed, Non-Alterable | GXN | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 25, 2026 | K253206 | METICULY Patient-specific CMF solution | JEY | Substantially Equivalent | Meticuly Co., Ltd. | accessdata.fda.gov |
| January 14, 2026 | K252958 | METICULY Patient-specific titanium mesh implant | GXN | Substantially Equivalent | Meticuly Co., Ltd. | accessdata.fda.gov |
| April 30, 2024 | K232889 | METICULY Patient-specific titanium maxillofacial mesh implant | JEY | Substantially Equivalent | Meticuly Co., Ltd. | accessdata.fda.gov |
| December 21, 2021 | K210099 | Meticuly Patient-Specific Titanium Mesh Implant | GXN | Substantially Equivalent | Meticuly Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated July 25, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.