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FDA 510(k)

INMODE WMBODY DEVICE

K-Number: K131362 · 2013-10-08

ApplicantInmode MD , Ltd.
Decision Date2013-10-08
Product CodeNUV
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INMODE WMBODY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Inmode MD , Ltd.. It received FDA 510(k) clearance on 2013-10-08 under 510(k) number K131362. The device is classified under product code NUV. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INMODE WMBODY DEVICE?

INMODE WMBODY DEVICE is a medical device that received FDA 510(k) clearance on 2013-10-08. The listed applicant is Inmode MD , Ltd.. The 510(k) number is K131362.

When did INMODE WMBODY DEVICE receive FDA 510(k) clearance?

INMODE WMBODY DEVICE received FDA 510(k) clearance on 2013-10-08, under 510(k) number K131362.

Who is the listed applicant for INMODE WMBODY DEVICE?

The FDA 510(k) record lists Inmode MD , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INMODE WMBODY DEVICE?

The FDA product code for INMODE WMBODY DEVICE is NUV.

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Other records listing Inmode MD , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: NUV)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261582Vacuum Roller RF Slimming Device for Medical Use (PZ-FY66-01, PZ-FY66-02)Zhengzhou PZ Laser Slim Technology Co., Ltd.K231092T-SHAPE 2B&M S.R.L. Marketing Nel BenessereK211272ICOONE Laser Med (also referred to as ICOONE Medical laser)I-Tech Industries SrlK182453ICOONE h (also referred to as ICOONE LASER and ICOONE –h LASER)I-Tech Industries SrlK161892Slimming Treatment DeviceBeijing Honkon Technologies Co., Ltd.K122579VELASHAPESyneron Medical, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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