Product code DZD— Dental

FDA has cleared 8 devices under product code DZD between 1978 and 1995, filed by 7 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.

• 19951 clearance
• 19942 clearances
• 19911 clearance
• 19901 clearance
• 19842 clearances
• 19781 clearance

• Alexotek Co.2 clearances
• Rocky Mountain Orthodontics, Inc.1 clearance
• Percussionaire Corp.1 clearance
• Ortho Specialties1 clearance
• Jon-Ko Products, Inc.1 clearance
• Dentauraum, Inc.1 clearance
• Aequitron Medical, Inc.1 clearance

• K943421 — ORTHODONITC ELASTOMERIC SLEEVINGJon-Ko Products, Inc.·1995-05-23
• K936243 — REGENCY TUBEOrtho Specialties·1994-02-02
• K935143 — DENTAURUM STAINLESS STEEL TUBINGDentauraum, Inc.·1994-01-31
• K911399 — NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)Aequitron Medical, Inc.·1991-09-19
• K896586 — RATE INCREASE FOR IPPB/IPVPercussionaire Corp.·1990-01-09
• K834446 — ALEXOTEK LINGUAL TUBESAlexotek Co.·1984-04-05
• K834392 — LABIAL CUSPID TUBEAlexotek Co.·1984-02-28
• K780205 — ORTHODONTIC BUCCAL TUBERocky Mountain Orthodontics, Inc.·1978-02-16