# K991015: LM-70 (Lidofilcon a) Spherical and Toric Soft Contact Lens for Daily Wear (Clear, Lathe-Cut)

- Pathway: 510(k) (Traditional)
- Applicant: Lamda Polytech, Ltd.
- Decided: Nov 2, 1999 after 221 days
- Product code: LPL (Lenses, Soft Contact, Daily Wear)
- Device class: 2
- Regulation: 21 CFR 886.5925
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) L1-70 (lidofilcon A): named in the summary without a submission number

## Indications for use
The LM-70 (lidofilcon A) Spherical Soft Contact Lens for daily wear are indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit refractive astigmatism of 0.75 diopters or less that does not interfere with visual acuity. The lens may be disinfected using either a chemical or heat disinfecting system. The LM-70 (lidofilcon A) Toric Soft Contact Lens for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes that are myopic or hyperopic and/or possesses refractive astigmatism not exceeding 10 diopters. The lens may be disinfected using either a chemical or heat disinfecting system.

Source page: https://510kreport.com/device/K991015
Methodology: https://510kreport.com/methodology