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Sign in to claim this brandTAKAYAMA INSTRUMENTS INC.
US
Last updated May 23, 2026
What TAKAYAMA INSTRUMENTS INC. makes
Takayama Instruments Inc. manufactures reusable surgical instruments, including forceps for soft-tissue manipulation, needle holders for suturing, irrigation/aspiration cannulas and handpieces, scissors, rongeurs for craniofacial procedures, and open-surgery dissectors. These tools are designed for general surgical use, with specific models like the Super Bypass and Kamiyama series. The company also produces irrigation system nozzles for surgical procedures.
All devices from Takayama Instruments Inc. fall under Class I regulation in the US, with product listings maintained in the FDA’s Unique Device Identifier (UDI) database. The company is headquartered in the United States, adhering to applicable regulatory requirements for reusable surgical instruments.
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 Takayama Instruments Inc. manufacture?
Takayama Instruments Inc. specializes in reusable surgical instruments, including forceps for manipulating soft tissue, needle holders for suturing, irrigation/aspiration cannulas and handpieces, general-purpose surgical scissors, craniofacial rongeurs, and open-surgery dissectors. These tools are designed for general surgical applications, with specific product lines like the Super Bypass and Kamiyama series. The company also produces irrigation system nozzles for surgical procedures.
Where is Takayama Instruments Inc. based?
Takayama Instruments Inc. is headquartered in the United States. The company operates within the regulatory framework of the country, ensuring compliance with applicable standards for reusable surgical instruments.
Which regulatory registries list Takayama Instruments Inc.’s devices?
Takayama Instruments Inc.’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 US, ensuring transparency and traceability for healthcare providers and regulators.
How are Takayama Instruments Inc.’s devices classified under US regulations?
All devices manufactured by Takayama Instruments Inc. fall under Class I regulation in the US. This classification applies to low-risk surgical instruments, including reusable tools like forceps, scissors, and irrigation systems, which are generally considered safe and effective with minimal regulatory oversight beyond basic manufacturing controls.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 707948014
Catalogue (179)
Page 3 of 4| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Kamiyama | KP-S02-18 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-13012 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-SET-MY22L | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-13030 | FDA UDI | Class I | Active |
| Super Bypass | SB-16NC | FDA UDI | Class I | Active |
| Super Bypass | SBTi-70FC | FDA UDI | Class I | Active |
| Kamiyama | K-804 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-07020 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-11015 | FDA UDI | Class I | Active |
| iON | iON-70-G | FDA UDI | Class I | Active |
| Kamiyama | K-8220 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-MY22 | FDA UDI | Class I | Active |
| Super Bypass | SBTi-70N-60 | FDA UDI | Class I | Active |
| Kamiyama | TK-20BR-AS | FDA UDI | Class I | Active |
| Super Bypass | SSTi-029 | FDA UDI | Class I | Active |
| Super Bypass | SBTi-1207 | FDA UDI | Class I | Active |
| Kamiyama | K-102-1 | FDA UDI | Class I | Active |
| Kamiyama | K-1030 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-032 | FDA UDI | Class I | Active |
| Kamiyama | K-3030-18 | FDA UDI | Class I | Active |
| Kamiyama | K-203 | FDA UDI | Class I | Active |
| Kamiyama | K-103-18 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-07015 | FDA UDI | Class I | Active |
| Super Bypass | SB-1610-MTL | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-18012 | FDA UDI | Class I | Active |
| Super Bypass | SB-90N-45 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-07012 | FDA UDI | Class I | Active |
| iON | iON-90-L | FDA UDI | Class I | Active |
| Super Bypass | SSTi-SET1L | FDA UDI | Class I | Active |
| Super Bypass | SB-70N-60 | FDA UDI | Class I | Active |
| Kamiyama | K-101-1 | FDA UDI | Class I | Active |
| Super Bypass | SBTi-70FS | FDA UDI | Class I | Active |
| Super Bypass | SB-16NC-MZ-L1 | FDA UDI | Class I | Active |
| Kamiyama | MT-15-C15 | FDA UDI | Class I | Active |
| Kamiyama | KTP-340 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-16020 | FDA UDI | Class I | Active |
| Kamiyama | K-815 | FDA UDI | Class I | Active |
| Kw | KW-90TF | FDA UDI | Class I | Active |
| Kamiyama | K-3030 | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-16030 | FDA UDI | Class I | Active |
| Super Bypass | SB-90FC | FDA UDI | Class I | Active |
| Super Bypass | SB-110N-60 | FDA UDI | Class I | Active |
| iON | iON-70 | FDA UDI | Class I | Active |
| Kamiyama | MT-25-S | FDA UDI | Class I | Active |
| Super Bypass | SBTi-110N-30-S | FDA UDI | Class I | Active |
| Super Bypass | SSTi-01-18030 | FDA UDI | Class I | Active |
| Super Bypass | SBTi-90FS | FDA UDI | Class I | Active |
| Super Bypass | SB-1610 | FDA UDI | Class I | Active |
| Kamiyama | K-110-1 | FDA UDI | Class I | Active |
| Kamiyama | K-808 | FDA UDI | Class I | Active |
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