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FDA 510(k)

IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022

K-Number: K231717 · 2023-09-06

Decision Date2023-09-06
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 is a medical device manufactured by Foshan Jindi Electric Appliance Co., Ltd.. It received FDA 510(k) clearance on 2023-09-06 under approval number K231717. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022?

IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 is a medical device that received FDA 510(k) clearance on 2023-09-06. It is manufactured by Foshan Jindi Electric Appliance Co., Ltd.. The 510(k) number is K231717.

When was IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 approved by the FDA?

IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 received FDA 510(k) clearance on 2023-09-06, under approval number K231717.

What company makes IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022?

IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 is manufactured by Foshan Jindi Electric Appliance Co., Ltd..

What is the FDA product code for IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022?

The FDA product code for IPL Home Use Hair Removal Device, Model(s): JD-TM002, JD-TM003, JD-TM012, JD-TM016, JD-TM022 is OHT.

Related Clinical Trials

Related PubMed Literature

Other Devices by Foshan Jindi Electric Appliance Co., Ltd.

Related Devices (Code: OHT)

Official Source

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