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

MOLLI 2 System

K Number: K253888 · Decision Dec 31, 2025
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
101
Review Days
27

Basic Information

Device Name
MOLLI 2 System
K Number
K253888
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
December 4, 2025
Decision Date
December 31, 2025
Product Code
NEU
Advisory Committee
General, Plastic Surgery
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
NEU Marker, Radiographic, Implantable

Similar 510(k) Clearances

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

View all

Other Clearances by Stryker Endoscopy

K Number Device Name
K253602 Precision S 4K Sinuscope
K261037 780 nm SPY Portable Handheld Imaging (SPY-PHI) System
K260185 1688 4K Camera System with Advanced Imaging Modality; 1788 4K Camera System with Advanced Imaging Modality
K260108 L12 LED Light Source with AIM
K254014 Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
K252010 SPY Laparoscope
K252012 SPY Cystoscope/Hysteroscope
K250544 Knotilus+ Biocomposite Knotless Anchor
K250528 Stryker AlphaVent™ Knotless SP Biocomposite Anchor
K241401 Connected OR Hub with Device and Voice Control; SDC4K Information Management System with Device and Voice Control
Search all 101 clearances from Stryker Endoscopy →