FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

TearCare MGX System

K Number: K252409 · Decision Apr 27, 2026
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
11
Applicant Total
11
Review Days
269

Basic Information

Device Name
TearCare MGX System
K Number
K252409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.5200
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sight Sciences, Inc.
Date Received
August 1, 2025
Decision Date
April 27, 2026
Product Code
ORZ
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
ORZ Eyelid Thermal Pulsation System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ORZ), ordered by most recent decision date.

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Other Clearances by Sight Sciences, Inc.

K Number Device Name
K242786 TearCare MGX System
K231084 TearCare MGX System
K232214 OMNI Surgical System
K213045 TearCare System
K202678 OMNI Surgical System
K201953 OMNI PLUS Surgical System
K173332 OMNI Surgical System
K171905 VISCO 360 Viscosurgical System
K143205 Viscoelastic Injector
K132494 VISCOELASTIC INJECTOR
Search all 11 clearances from Sight Sciences, Inc. →