Product code KDG— General, Plastic Surgery

FDA has cleared 11 devices under product code KDG between 1978 and 1995, 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.

• 19952 clearances
• 19892 clearances
• 19872 clearances
• 19841 clearance
• 19784 clearances

• Edward Weck, Inc.3 clearances
• Waterstone Medical, Inc.1 clearance
• Sil-Med Corp.1 clearance
• Porex Medical1 clearance
• Orthopedic Equipment Co., Inc.1 clearance
• Military Engineering, Inc.1 clearance
• Fdt Precision Machine Co., Inc.1 clearance
• Cher Mel Corp.1 clearance
• Avail-Southwest Division1 clearance

• K952678 — STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KITAvail-Southwest Division·1995-07-10
• K952200 — OMNI-JUGWaterstone Medical, Inc.·1995-06-29
• K894785 — SURGICAL CHISEL/OSTEOTOMEFdt Precision Machine Co., Inc.·1989-08-18
• K891471 — SIL-MED WASTE FLUID DUMP BAGSil-Med Corp.·1989-08-15
• K872947 — POREX QUALITY PLASTIC SURGERY INSTRUMENTSPorex Medical·1987-08-21
• K872092 — OSTEOTOME SET, HOKE, STRAIGHT, SET OF 5Military Engineering, Inc.·1987-06-23
• K842824 — CHERMEL BONE CHISELSCher Mel Corp.·1984-08-02
• K772373 — ANDERSON-NEIVERT OSTEOTOMEEdward Weck, Inc.·1978-03-09
• K772374 — SILVER OSTEOTOMEEdward Weck, Inc.·1978-03-09
• K772376 — NEIVERT OSTEOTOMEEdward Weck, Inc.·1978-03-09
• K780135 — CEMENT EXTRACTION INSTRUMENT SETOrthopedic Equipment Co., Inc.·1978-01-31