Product code GEJ— General, Plastic Surgery

FDA has cleared 5 devices under product code GEJ between 1987 and 2024, filed by 4 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

• 20241 clearance
• 19902 clearances
• 19881 clearance
• 19871 clearance

• Solos Endoscopy, Inc.2 clearances
• Cypris Medical1 clearance
• Cox-Uphuff Intl.1 clearance
• Cook Ob/Gyn1 clearance

• K240185 — Cypris eXact Suture Placement DeviceCypris Medical·2024-05-03
• K900958 — GS-1300 ATRAUMATIC GRASPING FORCEP, CURVED, 10MMSolos Endoscopy, Inc.·1990-04-18
• K900959 — GS-1400 TOOTHED DISSECTING FORCEP, 5MM, INSULATEDSolos Endoscopy, Inc.·1990-04-18
• K884553 — STAMEY NEEDLECook Ob/Gyn·1988-11-14
• K874342 — LIGATURE CARRIER/PACKER, HYDROXYLAPATITECox-Uphuff Intl.·1987-11-13