Is this your brand? Sign in to claim ownership.
Sign in to claim this brandMICROWARE PRECISION CO., LTD.
US
Last updated May 26, 2026
What MICROWARE PRECISION CO., LTD. makes
Microware Precision Co., Ltd. manufactures orthopaedic fixation devices, including non-sliding bone screws, non-bioabsorbable fixation plates, and reusable surgical tools like fluted drill bits and screwdrivers. Their portfolio includes locking plate systems and compression screw systems designed for bone stabilization. These products are used in orthopaedic procedures to support fracture fixation and bone alignment.
The company’s devices are classified under FDA categories Class I and Class II, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Microware Precision Co., Ltd. manufacture?
Microware Precision Co., Ltd. specializes in orthopaedic fixation devices. Their primary products include non-sliding bone screws, non-bioabsorbable fixation plates, reusable fluted surgical drill bits, and reusable surgical screwdrivers. These devices are designed for bone stabilization, fracture fixation, and alignment in orthopaedic surgeries.
Where is Microware Precision Co., Ltd. based?
The company is headquartered in the United States. This location is relevant for regulatory and compliance purposes, as it influences the jurisdiction under which their devices may be authorized.
Which regulatory registries list Microware Precision Co., Ltd.’s devices?
Microware Precision Co., Ltd.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the United States, ensuring transparency and traceability in the supply chain.
How are Microware Precision Co., Ltd.’s devices classified under FDA regulations?
Microware Precision Co., Ltd.’s devices fall under FDA Class I and Class II classifications. Class I devices generally pose minimal risk and may require less regulatory oversight, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification determines the regulatory pathway for authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- microware.com.tw
- —
- —
- [email protected]
- Phone
- +886424636275
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 658650833
Catalogue (2403)
Page 36 of 49Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Microware Precision Co., Ltd. Taichung · TW FEI 3007738812