# Meticuly Co., Ltd.

- Location (FDA's records): Bangkok, TH
- FDA decisions: 4 (2021–2026): 4 510(k) clearances
- Product codes: GXN (2), JEY (2)
- 510(k) review time since 2016: median 264 days, against 176 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Jeil Medical Corporation: 1 (https://510kreport.com/company/jeil-medical)
- Materialise NV: 1 (https://510kreport.com/company/materialise)
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)

## Firms that cite its devices most
- CG Bio Co., Ltd.: 1 (https://510kreport.com/company/cg-bio)

## Its most-cited devices
- K210099: Meticuly Patient-Specific Titanium Mesh Implant (2021), cited by 2

## Recent decisions
- K253206: METICULY Patient-specific CMF solution (Jul 25, 2026)
- K252958: METICULY Patient-specific titanium mesh implant (Jan 14, 2026)
- K232889: METICULY Patient-specific titanium maxillofacial mesh implant (Apr 30, 2024)
- K210099: Meticuly Patient-Specific Titanium Mesh Implant (Dec 21, 2021)

Source page: https://510kreport.com/company/meticuly