Last synced on 2 December 2022 at 11:04 pm

EarLens Contact Hearing Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150002
510(k) Type
Direct
Applicant
EARLENS CORPORATION
Country
United States
FDA Decision
Deleted
Decision Date
9/29/2015
Days to Decision
270 days

EarLens Contact Hearing Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN150002
510(k) Type
Direct
Applicant
EARLENS CORPORATION
Country
United States
FDA Decision
Deleted
Decision Date
9/29/2015
Days to Decision
270 days