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Sign in to claim this brandCameron-Miller, Inc.
US
Last updated May 23, 2026
What Cameron-Miller, Inc. makes
Cameron-Miller, Inc. manufactures reusable electrosurgical devices including monopolar and bipolar electrodes for endoscopic and open surgery, reusable electrosurgical handpieces, electrosurgical system generators, reusable return electrodes, and electrosurgical cable adaptors.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. Cameron-Miller, Inc. 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 devices does Cameron-Miller, Inc. manufacture?
Cameron-Miller, Inc. manufactures reusable electrosurgical devices, including monopolar and bipolar electrodes for endoscopic and open surgery, reusable electrosurgical handpieces, electrosurgical system generators, reusable return electrodes, and electrosurgical cable adaptors. These products are designed for use in surgical procedures where controlled electrical energy is applied to tissue for cutting, coagulation, or ablation. The company focuses exclusively on reusable electrosurgical components and systems, as specified in the provided device categories and summary.
Where is Cameron-Miller, Inc. based?
Cameron-Miller, Inc. is based in the United States, as explicitly stated in the SUMMARY section of the device data. The company's country of origin is listed as US, indicating its primary operational and legal jurisdiction is within the United States. This information is derived directly from the provided data and does not include any inference about specific states, cities, or facilities beyond the national designation.
Which regulatory registries list Cameron-Miller, Inc.'s devices?
Cameron-Miller, Inc.'s devices are listed in the FDA 510(k) and FDA UDI registries, as indicated in the LISTED IN field of the device data. These registries are U.S. Food and Drug Administration systems used to track medical device submissions and unique device identifiers. The inclusion in these registries reflects that the company's devices have undergone FDA review processes, but it does not imply company-wide approval, as only individual devices may be authorized under these pathways.
How are Cameron-Miller, Inc.'s devices classified?
Cameron-Miller, Inc.'s devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the provided data. This classification reflects the level of regulatory control required to ensure safety and effectiveness, with Class I devices subject to general controls and Class II devices requiring additional special controls. The classification applies to individual devices within the company's product range, not the company as a whole, and is based on the intended use and risk profile of each device type.
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
- 051923530
Catalogue (141)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cameron-Miller | 26-0832 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-0854 | FDA UDI | Class II | Active |
| Cameron-Miller | 80-7120 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1104 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1612 | FDA UDI | Class II | Active |
| Cameron-Miller | 80-7105 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-2035 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1604 | FDA UDI | Class I | Active |
| Cameron-Miller | 75-2816 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1635 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-2925 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-2922 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1220 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-0859 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1949 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1943 | FDA UDI | Class II | Active |
| Cameron-Miller | 75-2813 | FDA UDI | Class II | Active |
| Cameron-Miller | 75-2812 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-0860 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-0941 | FDA UDI | Class II | Active |
| Cameron-Miller | 80-2123 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-2924 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-1895 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-2935 | FDA UDI | Class II | Active |
| Cameron-Miller | 26-0952 | FDA UDI | Class II | Active |
| Cameron-Miller | 80-7196 | FDA UDI | Class II | Active |
| Cameron-Miller | 80-7178 | FDA UDI | Class II | Active |
| Technicator | K812702 | FDA 510(k) | Class II | Active |
| Cameron-Miller #40-1516 | K822092 | FDA 510(k) | Class II | Active |
| Electrosurgical Generator | K771639 | FDA 510(k) | Class II | Active |
| Hand Control Access.-Electrosurg. Units | K772235 | FDA 510(k) | Class II | Active |
| Model 80-1765 Electrosurgical Unit | K791415 | FDA 510(k) | Class II | Active |
| Hand Controlled Pencil Or Switch Hand | K833449 | FDA 510(k) | Class II | Active |
| Papillotome Cutting Snare | K781353 | FDA 510(k) | Class II | Active |
| Electrosurgical Unit Model 26-0335 | K944775 | FDA 510(k) | Class II | Active |
| Fiber Optic Adjustable Headlight | K780433 | FDA 510(k) | Class II | Active |
| Model 80-1983, Electrosurgical Generator | K931437 | FDA 510(k) | Class II | Active |
| Electrosurgical Device, Model 26-2500 | K935490 | FDA 510(k) | Class II | Active |
| Cameron-Miller Model 80-2701, Bipolar Coagulator | K853972 | FDA 510(k) | Class II | Active |
| Model 26-0375, Electrosurgical Generator | K931541 | FDA 510(k) | Class II | Active |
| Electrosurgical Devices, 26-0330, 26-335, 340 & 0345 | K854109 | FDA 510(k) | Class II | Active |
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