Product code DYX— Dental
DENTAL ARCH BAR
- Classification name
- Lock, Wire, And Ligature, Intraoral
- Device class
- Class 2
- Regulation
- 21 CFR 872.4600
- Advisory panel
- Dental
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code DYX
FDA has cleared devices under product code DYX between 1982 and 2017, filed by 11 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2017
- 2006
- 2003
- 1999
- 1993
- 1991
- 1986
- 1982
Top applicants under product code DYX
Recent clearances under product code DYX
- K162046 — MINNE TIES MMF Suture System
- K061271 — ERCH ARCH BAR, MODEL 38-690-00
- K031207 — SAFETY RELEASE ARCH BAR KIT
- K030605 — RAPID IMF
- K990212 — LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00
- K991004 — SYNTHES QUICK LOCK IMF SYSTEM
- K925106 — IMPLANTABLE PULSE GENERATORS
- K925712 — RELIANCE SHORT STICK TIE
- K910090 — DIMAC WIRES
- K863799 — JAW FIXATION ASSEMBLY
- K820944 — DENTAL ARCH BAR
Data sourced from openFDA. This site is unofficial and independent of the FDA.