Product code GDL— General, Plastic Surgery

FDA has cleared 5 devices under product code GDL between 1981 and 1988, 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.

• 19881 clearance
• 19852 clearances
• 19821 clearance
• 19811 clearance

• Artiberia2 clearances
• S. Jackson, Inc.1 clearance
• Ortho Pared Instruments, Inc.1 clearance
• China National Medicines C/O Havel'S1 clearance

• K881394 — NON-STERILE SUTURE NEEDLESChina National Medicines C/O Havel'S·1988-04-08
• K851781 — 25-420 TO 25-436 VARIOUS TYPES OF SUTURE NEEDLESArtiberia·1985-06-20
• K851782 — 25-450 TO 25-540 VARIOUS SUTURE FORCEPSArtiberia·1985-06-20
• K813589 — SHARTPOINT EYED NEEDLESS. Jackson, Inc.·1982-01-18
• K812566 — UNIVERSAL SUTURE PASSEROrtho Pared Instruments, Inc.·1981-11-10