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NeuWave Medical, Inc.

United States·US-MF-000016783

Last updated September 17, 2026

What NeuWave Medical, Inc. makes

NeuWave Medical, Inc. makes endoscopic electrosurgical handpieces and electrodes that are bipolar and single-use, foot-switches for electrical control, microwave ablation system generators, microwave ablation system probes that are non-powered, and microwave ablation system probes with planar-coagulation guides.

The company's devices are classified as Class I, Class II, and Class IIb and are listed in the Eudamed, FDA 510(k), and FDA UDI registries. NeuWave Medical, 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 does NeuWave Medical, Inc. make?

Where is NeuWave Medical, Inc. based?

NeuWave Medical, Inc. is based in the United States, as explicitly stated in the device data under the COUNTRY field and confirmed in the summary.

Which registries list NeuWave Medical, Inc.'s devices?

NeuWave Medical, Inc.'s devices are listed in the Eudamed, FDA 510(k), and FDA UDI registries, as specified in the LISTED IN field of the device data.

How are NeuWave Medical, Inc.'s devices classified?

NeuWave Medical, Inc.'s devices are classified as Class I, Class II, and Class IIb, as directly stated in the DEVICE CLASSES field of the provided data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: United States
Address: 3529, Anderson Street, Madison, United States
Website: neuwave.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: —
PRRC Contact: Candace Peterson
EUDAMED SRN: US-MF-000016783
FDA FEI Number: 3008769756
DUNS Number: —

Catalogue (80)

Page 2 of 2

Device	Model / Reference	Registries	Class	Status
NEUWAVE Microwave Ablation System and Accessories	K200081	FDA 510(k)	Class II	Active
NEUWAVE™ Microwave Ablation System and Accessories	K231738	FDA 510(k)	Class II	Active
Certus 140 2.45ghz Ablation System	K122217	FDA 510(k)	Class II	Active
FLEX Microwave Ablation System and Accessories	K163118	FDA 510(k)	Class II	Active
Neuwave Ablate-Iq	NWACINT	EUDAMED	Class IIb	Active
Neuwave	NWC2KR1N	EUDAMED	Class IIb	Active
Neuwave	LK20XT	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	PD2MSURG	EUDAMEDFDA UDI	Class I	Active
Neuwave	PR15XT	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	FSWITCH1	EUDAMEDFDA UDI	Class I	Active
Neuwave	LN20	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	NWC2DE1N	EUDAMED	Class IIb	Active
Neuwave	FSWITCH2	EUDAMEDFDA UDI	Class I	Active
Neuwave	CTBKT4	EUDAMEDFDA UDI	Class I	Active
Neuwave	LN15	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	PR20XT	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	PRS15	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	PR15	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	LK15	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	NWC1US1N	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	LK20	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	CTBKT1	EUDAMEDFDA UDI	Class I	Active
Neuwave	NWC2FR1N	EUDAMED	Class IIb	Active
Neuwave	NWC2SG1N	EUDAMED	Class IIb	Active
Neuwave Ablate-Iq	AIQP	EUDAMED	Class IIb	Active
Neuwave	NWC2HK1N	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	NWC2IT1N	EUDAMED	Class IIb	Active
Neuwave	PR20	EUDAMEDFDA UDI	Class IIb	Active
Neuwave	NWC1CA1N	EUDAMED	Class IIb	Active
Neuwave	LK15XT	EUDAMEDFDA UDI	Class IIb	Active

Related Companies

Authorised Representatives

Johnson & Johnson Medical GmbH DE

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Authorities

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