Stryker Endoscopy - FDA 510(k) Cleared Devices
Recent clearances: AIR+ All-Inside Meniscal Repair Device, Curved Up, Precision S 4K Sinuscope, 780 nm SPY Portable Handheld Imaging (SPY-PHI) System
103
Total
102
Cleared
1
Denied
FDA 510(k) Regulatory Record - Stryker Endoscopy Orthopedic ✕
38 devices
Cleared
Jul 30, 2026
AIR+ All-Inside Meniscal Repair Device, Curved Up
Orthopedic
20d
Not Cleared
Jul 17, 2026
SportSuite Vision Software
Orthopedic
318d
Cleared
May 23, 2025
Knotilus+ Biocomposite Knotless Anchor
Orthopedic
87d
Cleared
May 21, 2025
Stryker AlphaVent™ Knotless SP Biocomposite Anchor
Orthopedic
86d
Cleared
Mar 07, 2024
ICONIX All-Suture Anchor
Orthopedic
27d
Cleared
Jan 25, 2024
AlphaVent Knotless SP PEEK Anchor
Orthopedic
48d
Cleared
Oct 24, 2023
Knotilus+ PEEK Knotless Anchor
Orthopedic
53d
Cleared
Aug 30, 2023
AlphaVent Suture Anchors
Orthopedic
134d
Cleared
Aug 04, 2021
Alpha Vent PEEK Suture Anchor
Orthopedic
82d
Cleared
Mar 11, 2021
Stryker ProCinch Adjustable Loop Device
Orthopedic
58d
Cleared
Apr 17, 2015
ProCinch Adjustable Loop Device
Orthopedic
58d
Cleared
Jan 09, 2013
STRYKER CROSSFLOW ARTHROSCOPY PUMP
Orthopedic
62d
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