Product code ECB— Dental
BRACE (ORAFIX SPECIAL)
- Classification name
- Unit, Syringe, Air And/Or Water
- Device class
- Class 1
- Regulation
- 21 CFR 872.4565
- Advisory panel
- Dental
- Total cleared
- 12
- First cleared
- Most recent
Market context for product code ECB
FDA has cleared devices under product code ECB between 1978 and 1994, filed by 12 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
- 1991
- 1989
- 1986
- 1980
- 1978
Top applicants under product code ECB
Recent clearances under product code ECB
- K942519 — UNI-SYRINGE, UNI-TIP AND ACCESS SYRINGE TIPS
- K931772 — SURETIP SYRINGE TIP COVER
- K931137 — DENTAL SYRINGE TIP
- K923876 — RISKONTROL SINGLE USE
- K923285 — PRO-TIP DISPOSABLE 3/1 SYRINGE NOZZLE
- K920499 — SANI-TIP
- K911756 — POSTERIOR NASAL EPISTAXIS INSTRUMENTS
- K890290 — BRACE (ORAFIX SPECIAL)
- K863024 — SERINGA TRIPLICE S.L.
- K854699 — TUBING SYRING
- K801686 — SPACELINE THREE WAY SYRINGE
- K781594 — DENTAL WARM WATER IRRIGATING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.