Last synced on 14 November 2025 at 11:06 pm

TFX-LT2000 Therapy Light

Page Type
Cleared 510(K)
510(k) Number
K211265
510(k) Type
Traditional
Applicant
ToeFX, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
570 days
Submission Type
Statement

TFX-LT2000 Therapy Light

Page Type
Cleared 510(K)
510(k) Number
K211265
510(k) Type
Traditional
Applicant
ToeFX, Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
11/17/2022
Days to Decision
570 days
Submission Type
Statement