Low Energy Direct Current Thermal Ablation System
FDA product code OAB · 14 cleared devices
Class 2
General, Plastic Surgery
- Regulation
- 21 CFR 878.4400
- Review panel
- SU
- Implant
- No
- Life sustaining
- No
- Third party review
- Yes
- GMP exempt
- No
- Clearance span
- 2006-11-21 – 2026-08-12
Ablation of soft tissue
OAB
2026-08-12
OAB
2026-05-07
Aliya® EX System; Aliya® EX Generator; Aliya® Needle; Aliya® Electrode; INUMI™ Flex Needle
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OAB
2026-03-24
NanoKnife Generator (H78720300351US0)
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OAB
2024-12-06
NanoKnife Generator (H78720300301US0); NanoKnife Single Electrode Activation Probe, 15 cm (H787204001090); NanoKnife Single Electrode Activation Probe, 25 cm (H787204001100); NanoKnife Single Electrode Probe Spacer (H787204003010)
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OAB
2024-10-04
Electroporation System (N3000)
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OAB
2024-05-22
INUMI™ Flex Needle
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OAB
2024-05-03
Canady Helios Cold Plasma™ XL-1000CP™ Ablation System (XL-1000CPSYS)
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OAB
2023-06-08
Irreversible Electroporation Ablation Generator, Irreversible Electroporation Probe
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OAB
2022-06-17
Aliya(TM) System, Aliya(TM) Generator, Aliya(TM) Needle, Aliya(TM) Electrode
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OAB
2019-06-18
NanoKnife System
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OAB
2011-10-24
NANOKNIFE SYSTEM
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OAB
2008-05-08
ONCOBIONIC SYSTEM WITH 6 PROBE OUTPUT
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OAB
2008-04-02
ONCOBIONIC SYSTEM
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OAB
2006-11-21
ONCOBIONIC SYSTEM
View details →No matching devices.
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