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Cameron-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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LinkedIn
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Facebook
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Email
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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 2 of 3
DeviceModel / ReferenceRegistriesClassStatus
Cameron-Miller 26-1229
FDA UDI
Class IIActive
Cameron-Miller 26-1230
FDA UDI
Class IIActive
Cameron-Miller 26-0991
FDA UDI
Class IIActive
Cameron-Miller 26-0869
FDA UDI
Class IIActive
Cameron-Miller 26-5574
FDA UDI
Class IActive
Cameron-Miller 80-1777
FDA UDI
Class IIActive
Cameron-Miller 80-7175
FDA UDI
Class IIActive
Cameron-Miller 26-1942
FDA UDI
Class IIActive
Cameron-Miller 26-1606
FDA UDI
Class IActive
Cameron-Miller 26-1009
FDA UDI
Class IIActive
Cameron-Miller 26-0865
FDA UDI
Class IIActive
Cameron-Miller 26-1941
FDA UDI
Class IIActive
Cameron-Miller 26-2108
FDA UDI
Class IIActive
Cameron-Miller 80-7117
FDA UDI
Class IIActive
Cameron-Miller 80-7026
FDA UDI
Class IIActive
Cameron-Miller 26-2947
FDA UDI
Class IIActive
Cameron-Miller 26-1632
FDA UDI
Class IIActive
Cameron-Miller 80-7172
FDA UDI
Class IIActive
Cameron-Miller 26-1232
FDA UDI
Class IIActive
Cameron-Miller 75-2802
FDA UDI
Class IIActive
Cameron-Miller 80-7145
FDA UDI
Class IIActive
Cameron-Miller 26-2926
FDA UDI
Class IIActive
Cameron-Miller 26-1063
FDA UDI
Class IIActive
Cameron-Miller 80-7214
FDA UDI
Class IIActive
Cameron-Miller 26-1615
FDA UDI
Class IIActive
Cameron-Miller 26-2015
FDA UDI
Class IIActive
Cameron-Miller 26-1109
FDA UDI
Class IIActive
Cameron-Miller 26-2914
FDA UDI
Class IIActive
Cameron-Miller 26-2957
FDA UDI
Class IIActive
Cameron-Miller 80-7176
FDA UDI
Class IIActive
Cameron-Miller 75-2817
FDA UDI
Class IIActive
Cameron-Miller 26-0863
FDA UDI
Class IIActive
Cameron-Miller 26-1896
FDA UDI
Class IIActive
Cameron-Miller 26-1233
FDA UDI
Class IIActive
Cameron-Miller 26-1894
FDA UDI
Class IIActive
Cameron-Miller 26-1992
FDA UDI
Class IIActive
Cameron-Miller 75-2814
FDA UDI
Class IIActive
Cameron-Miller 80-8008
FDA UDI
Class IIActive
Cameron-Miller 26-2051
FDA UDI
Class IIActive
Cameron-Miller 26-0335
FDA UDI
Class IIActive
Cameron-Miller 26-0375
FDA UDI
Class IIActive
Cameron-Miller 26-1121
FDA UDI
Class IIActive
Cameron-Miller 26-1021
FDA UDI
Class IIActive
Cameron-Miller 75-5751
FDA UDI
Class IIActive
Cameron-Miller 80-7116
FDA UDI
Class IIActive
Cameron-Miller 26-0867
FDA UDI
Class IIActive
Cameron-Miller 26-0365
FDA UDI
Class IIActive
Cameron-Miller 26-0992
FDA UDI
Class IIActive
Cameron-Miller 80-7102
FDA UDI
Class IIActive
Cameron-Miller 26-1224
FDA UDI
Class IIActive

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