Product code EGM— Dental
CYBERJET LOCAL ANESTHESIA SYSTEM
- Classification name
- Injector, Jet, Mechanical-Powered
- Device class
- Class 2
- Regulation
- 21 CFR 872.4475
- Advisory panel
- Dental
- Total cleared
- 11
- First cleared
- Most recent
Market context for product code EGM
FDA has cleared devices under product code EGM between 1979 and 2025, 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
- 2025
- 2010
- 1997
- 1996
- 1990
- 1987
- 1984
- 1982
- 1979
Top applicants under product code EGM
Recent clearances under product code EGM
- K243427 — QuickSleeper 5
- K083811 — W&H HANDPIECE ANESTO, MODEL: RA-5
- K964802 — CYBERJET LOCAL ANESTHESIA SYSTEM
- K962017 — HYPODERMIC JET INJECTION APPARATUS
- K904279 — PAROJECT ANESTHETIC SYRINGE
- K864294 — HENKE-JECT PRESSURE SYRINGE (MODIFICATION)
- K864732 — GRADTECH SYRINGE SYSTEM
- K864861 — INSTRUMENTATIONS UNLIMITED SYRINGE SYSTEM
- K834361 — JSB JET SYRINGE
- K821273 — MAYO SCISSOR STRAIGHT 6 3/4
- K790193 — MIZZY SYRIJET MARK IV
Data sourced from openFDA. This site is unofficial and independent of the FDA.