Skip to content

Glide Device

by Home Skinovations, Ltd. 2 variants

510(k) K131870

Glide Device is a medical device (FDA Class II; FDA product code OHT, Light Based Over-The-Counter Hair Removal) made by Home Skinovations, Ltd., cleared under FDA 510(k) K131870 on 14 Aug 2013, 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 · Special NumberK131870 Date14 Aug 2013ClearedStatusActive

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  • Withdrawn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
OHT
FDA applicant
Home Skinovations , Ltd.
Device class
Class II
Regulation
21 CFR Part 878.4810
Advisory committee
General, Plastic Surgery
FDA decision
SESE Substantially Equivalent

Related clearances

cited in the FDA summary

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

Cites

Cited by

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

Similar devices

Other devices filed under FDA product code OHT (Light Based Over-The-Counter Hair Removal).

Other devices from Home Skinovations, Ltd.

See all devices from Home Skinovations, Ltd. →