Product code GDG— General, Plastic Surgery

FDA has cleared 10 devices under product code GDG between 1977 and 1990, filed by 8 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.

• 19901 clearance
• 19891 clearance
• 19861 clearance
• 19842 clearances
• 19811 clearance
• 19791 clearance
• 19781 clearance
• 19772 clearances

• Edward Weck, Inc.3 clearances
• Zinnanti Surgical Instruments, Inc.1 clearance
• Xomed, Inc.1 clearance
• United States Surgical, A Division of Tyco Healthc1 clearance
• Premier Dental Products Co.1 clearance
• Humboldt Products1 clearance
• Cedar Surgical, Inc.1 clearance
• Brimfield Scientific Instruments1 clearance

• K900069 — MODIFIED PGL ABSORBABLE STAPLE*United States Surgical, A Division of Tyco Healthc·1990-04-16
• K891898 — SKIN HOOKS, VARIOUS TYPESZinnanti Surgical Instruments, Inc.·1989-04-12
• K864425 — RAYLOR(TM) DISSECTING HOOKCedar Surgical, Inc.·1986-12-12
• K843136 — BRIMFIELD CANNULATED GRASPING HOOKSBrimfield Scientific Instruments·1984-09-25
• K841010 — SURGICAL HOOKS, VARIOUSPremier Dental Products Co.·1984-05-01
• K812562 — SURGICAL RETRACTOR & ELASTIC STAYS, DISPHumboldt Products·1981-10-02
• K791120 — MIDDLE EAR PICKS, HOOKS CURETTES,Xomed, Inc.·1979-07-10
• K780289 — NERVE APPROXIMATEREdward Weck, Inc.·1978-06-14
• K771187 — DERMAHOOK #382-805Edward Weck, Inc.·1977-07-11
• K771190 — ABRAMSON TRACHEA HOOK & RETRACTOREdward Weck, Inc.·1977-07-11