Product code JYG— Ear, Nose, Throat

FDA has cleared 7 devices under product code JYG between 1982 and 1993, filed by 5 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
• 19842 clearances
• 19831 clearance
• 19822 clearances

• Treace Medical, Inc.2 clearances
• Kelleher Corp.2 clearances
• Premier Dental Products Co.1 clearance
• Ear Tech, Inc.1 clearance
• Bionix Corp.1 clearance

• K932609 — EAR CURETTEEar Tech, Inc.·1993-07-21
• K852039 — FLEX-LOOP FLEXIBLE EAR CORETTEBionix Corp.·1985-06-11
• K841354 — CURETTETreace Medical, Inc.·1984-07-06
• K841001 — EAR CURETTE, VARIOUSPremier Dental Products Co.·1984-05-29
• K823916 — WAX CURETTE TIPTreace Medical, Inc.·1983-01-21
• K822273 — ENT CURRETTESKelleher Corp.·1982-08-30
• K822006 — OPERATIVE EAR CURRETTES & RELATED ITEMKelleher Corp.·1982-08-12