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sensiLift

by El Global Trade Ltd

510(k) K170499

sensiLift is a Class II device made by El Global Trade Ltd, cleared under FDA 510(k) K170499 on 15 Jun 2017, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK170499 Date15 Jun 2017ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
PAY
FDA applicant
El Global Trade, Ltd.
Device class
Class II
Regulation
21 CFR Part 878.4420
Advisory committee
General, Plastic Surgery
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Devices cleared under K170499

2 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K170499
UDI-DISize and differences
sensiLift ST100US01SNS
EL GLOBAL TRADE LTD
ST100US01SNS05060445341125 —On the market
Sensilift ST100US04SNS
EL GLOBAL TRADE LTD
ST100US04SNS05060445341255 —On the market

Similar devices

Other devices filed under FDA product code PAY (Over-The-Counter Radiofrequency Coagulation Device For Wrinkle Reduction).

Other devices from El Global Trade Ltd.

See all devices from El Global Trade Ltd. →