DZA · Class I · 21 CFR 872.4130

FDA Product Code DZA: Drill, Dental, Intraoral

Leading manufacturers include Tulsa Dental Products, Ltd., Del Medical Systems Corp. and W&H Dentalwerk Buermoos GmbH.

13

Total

13

Cleared

119d

Avg days

1976

Since

FDA 510(k) Cleared Drill, Dental, Intraoral Devices (Product Code DZA)

13 devices

1–13 of 13

Cleared Jun 25, 1999

SURGICAL CONTRA-ANGLE HANDPIECES, MODELS 975 AE,979 E/KM, 985 AE, 986 AE, 988 E/KM AND SURGICAL STRAIGHT HANDPIECES MOD

W&H Dentalwerk Buermoos GmbH

Cleared Sep 25, 1996

S-53 INTRORAL DENTAL SYSTEM

Del Medical Systems Corp.

Cleared Jan 16, 1996

PROFILE NICKEL TITANIUM ROTARY INSTRUMENTS

Tulsa Dental Products, Ltd.

Cleared Apr 25, 1990

Ivoclar North America, Inc.

Cleared Dec 23, 1976

AIROTOS LF HANDPIECE

About Product Code DZA - Regulatory Context

Related FDA 510(k) Regulatory Insights

Data Source

FDA 510(k) public files . 176,325 total devices indexed.

Latest clearance: Jun 25, 1999

Product Code Info

Code	DZA
Device class	Class I
CFR	21 CFR 872.4130
Panel	Dental

Verify on FDA.gov

View DZA classification on FDA.gov →