← FDA Medical Device Classifications

Lenses, Soft Contact, Daily Wear

LPL · Class II — Moderate Risk (510(k) clearance required) · Ophthalmic · 21 CFR 886.5925

Classification

FDA Product Code

LPL

Device class

Class II — Moderate Risk (510(k) clearance required)

Regulation

21 CFR 886.5925

Review panel

OP

Medical specialty

Ophthalmic

Submission type

1

GMP exempt

N

Life sustaining

N

Implant

N

Third-party review

Y

Market data

Cleared 510(k) submissions

483

Registered establishments

128

Source

Authoritative

FDA Device Classification database

Machine

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