Micro-Tech Medical Technology (Thailand) Co., Ltd.
2 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (2)
Devices registered here (1)
- Snare, SurgicalProduct code GAE (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800
Recalls & enforcement
- Class IITerminated2018-09-20Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units
- Class IITerminated2018-03-12The combination of the firmness of the mass, the potential endoscope and elevator position combined with the force required to penetrate the mass may contribute to the breakage of the needle in the human body, which could cause injury.
Related
- All facilities operated by Micro-Tech (Nanjing) Co., Ltd.
- Micro-Tech (Nanjing) Co., Ltd. (CN)
- Micro-Tech (Nanjing) Co., Ltd. (CN)
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Micro-Tech Medical Technology (Thailand) Co., Ltd. (FEI 3046205723) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3046205723-micro-tech-medical-technology-thailand-c/
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