Last synced on 25 January 2026 at 3:41 am

OBERON: LASER SURGERY FIBER, ATRAUMATIC SURGERY FIBER, SIDE FIRE FIBER, RADIAL EMISSION FIBER, DENTAL SURGERY FIBER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140470
510(k) Type
Traditional
Applicant
Oberon GmbH Fiber Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2014
Days to Decision
232 days
Submission Type
Summary

OBERON: LASER SURGERY FIBER, ATRAUMATIC SURGERY FIBER, SIDE FIRE FIBER, RADIAL EMISSION FIBER, DENTAL SURGERY FIBER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140470
510(k) Type
Traditional
Applicant
Oberon GmbH Fiber Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2014
Days to Decision
232 days
Submission Type
Summary