Product code EGN— Dental

FDA has cleared 7 devices under product code EGN between 1982 and 1993, filed by 3 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.

• 19931 clearance
• 19851 clearance
• 19825 clearances

• Conphar, Inc.5 clearances
• Gendex Corp.1 clearance
• Artiberia1 clearance

• K932675 — GXP DENTAL X-RAY PROCESSORGendex Corp.·1993-07-26
• K851720 — 1155/1 TO 1162/12 VARIOUS TYPES GUM SCISSORSArtiberia·1985-07-02
• K821275 — MAYO SCISSOR STRAIGHT 5 1/2Conphar, Inc.·1982-05-28
• K821276 — MAYO SCISSOR CURYED 5 1/2Conphar, Inc.·1982-05-28
• K821292 — TONSIL SCISSORS 7Conphar, Inc.·1982-05-28
• K821294 — TONSIL SCISSORS STRAIGHT 5 1/2Conphar, Inc.·1982-05-28
• K821077 — CONPHARConphar, Inc.·1982-05-24