Product code GEG— General, Plastic Surgery

FDA has cleared 12 devices under product code GEG between 1978 and 1989, filed by 9 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.

• 19895 clearances
• 19874 clearances
• 19861 clearance
• 19841 clearance
• 19781 clearance

• Kinetic Medical Products3 clearances
• Zinnanti Surgical Instruments, Inc.2 clearances
• Orthopedic Systems, Inc.1 clearance
• Orthopedic Equipment Co., Inc.1 clearance
• Military Engineering, Inc.1 clearance
• Micro-Aire Surgical Instruments, Inc.1 clearance
• Imm Enterprises , Ltd.1 clearance
• Cedar Surgical, Inc.1 clearance
• Buckman Co., Inc.1 clearance

• K891894 — ELEVATORS-COTTLE,MCKENTY,GOLDMAN,JOSEPH,CONVERSEZinnanti Surgical Instruments, Inc.·1989-04-12
• K891899 — ELEVATORS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.·1989-04-12
• K890365 — SEPTUM ELEVATORKinetic Medical Products·1989-02-03
• K890230 — LIGATURE NEEDLESKinetic Medical Products·1989-01-27
• K890253 — SURGICAL ELEVATORKinetic Medical Products·1989-01-27
• K872491 — 1.1 TWIST DRILLS AND 1.2 CORTICAL DRILLSMicro-Aire Surgical Instruments, Inc.·1987-07-16
• K870781 — ACROMED WALLIE-HEINIG DISECTOR/ELEVATORSBuckman Co., Inc.·1987-03-09
• K870591 — ELEVATOR, COBB SPINALMilitary Engineering, Inc.·1987-02-26
• K870126 — FEMUR WRENCHOrthopedic Systems, Inc.·1987-02-03
• K864421 — RAYLOR(TM) PERIOSTEAL ELEVATORSCedar Surgical, Inc.·1986-11-26
• K834176 — H.R. JAKOBI SURG. INSTRUMENTS 40/41Imm Enterprises , Ltd.·1984-01-27
• K781449 — HARRINGTON SPINAL ELEVATOROrthopedic Equipment Co., Inc.·1978-09-27