Stryker Endoscopy - FDA 510(k) Cleared Devices
99
Total
99
Cleared
0
Denied
Stryker Endoscopy has 99 FDA 510(k) cleared medical devices. Based in San Jose, US.
Latest FDA clearance: Feb 2026. Active since 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Stryker Endoscopy Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Stryker Endoscopy
99 devices
Cleared
Feb 18, 2026
1688 4K Camera System with Advanced Imaging Modality
General & Plastic Surgery
28d
Cleared
Feb 12, 2026
L12 LED Light Source with AIM
General & Plastic Surgery
29d
Cleared
Jan 13, 2026
Connected OR Hub with Device and Voice Control
General & Plastic Surgery
29d
Cleared
Dec 31, 2025
MOLLI 2 System
General & Plastic Surgery
27d
Cleared
Jul 24, 2025
SPY Laparoscope
General & Plastic Surgery
27d
Cleared
Jul 18, 2025
SPY Cystoscope/Hysteroscope
Obstetrics & Gynecology
21d
Cleared
May 23, 2025
Knotilus+ Biocomposite Knotless Anchor
Orthopedic
87d
Cleared
May 21, 2025
Stryker AlphaVent™ Knotless SP Biocomposite Anchor
Orthopedic
86d
Cleared
Aug 15, 2024
Connected OR Hub with Device and Voice Control
General & Plastic Surgery
90d
Cleared
Mar 07, 2024
ICONIX All-Suture Anchor
Orthopedic
27d
Cleared
Feb 22, 2024
1688 4K Camera System with Advanced Imaging Modality
General & Plastic Surgery
30d
Cleared
Feb 12, 2024
SPY Cystoscope/Hysteroscope
Obstetrics & Gynecology
91d
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