Product code DYN— Dental
SALIVA EJECTOR
- Classification name
- Mouthpiece, Saliva Ejector
- Device class
- Class 1
- Regulation
- 21 CFR 872.6640
- Advisory panel
- Dental
- Total cleared
- 18
- First cleared
- Most recent
Market context for product code DYN
FDA has cleared devices under product code DYN between 1976 and 1994, filed by 18 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.
Clearances per year
- 1994
- 1993
- 1992
- 1990
- 1987
- 1986
- 1980
- 1978
- 1976
Top applicants under product code DYN
Recent clearances under product code DYN
- K940769 — DENTFLEX DISPLOSABLE DENTAL SALIVA EJECTOR
- K935616 — SALIVA EJECTOR DISPOSABLE
- K935758 — HYGOFLEX SALIVA-EJECTOR
- K924211 — EJECTOR
- K920492 — HIGH VAC
- K921117 — MINIDAM
- K900631 — SALIVA ABSORBER - DENTAL
- K871315 — ORAL ASPIRATOR
- K870599 — TIP, DENTAL SUCTION APPARATUS
- K864300 — SILIVA EJECTOR/ORAL CAVITY EVACUATOR
- K863768 — SALIVA EJECTORS
- K863163 — ULS 8-86
- K861934 — SALIVA EJECTOR
- K801927 — SILENTSLEEP
- K800210 — TONGUE HOLDER/SALIVA EJECTOR
- K781592 — SURGICAL ASPIRATOR TIPS
- K761264 — OPTIONS FOR STAR DENTAL OPUS I
- K760620 — SALIVA EJECTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.