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

L12 LED Light Source with AIM

K Number: K260108 · Decision Feb 12, 2026
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
60
Applicant Total
101
Review Days
29

Basic Information

Device Name
L12 LED Light Source with AIM
K Number
K260108
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
January 14, 2026
Decision Date
February 12, 2026
Product Code
OWN
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
OWN Confocal Optical Imaging

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