← Product Code [EGM](/submissions/DE/subpart-e%E2%80%94surgical-devices/EGM) · K964802 # CYBERJET LOCAL ANESTHESIA SYSTEM (K964802) _Intra Vantage, Inc. · EGM · May 27, 1997 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGM/K964802 ## Device Facts - **Applicant:** Intra Vantage, Inc. - **Product Code:** [EGM](/submissions/DE/subpart-e%E2%80%94surgical-devices/EGM.md) - **Decision Date:** May 27, 1997 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.4475 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** Therapeutic ## Intended Use Administration of intraosseous anesthesia for dental indications. ## Device Story Cyberjet™ is a dental device for intraosseous local anesthesia. It integrates a drill and an injection needle into a single unit. The dentist identifies an injection site, applies topical anesthetic, and uses the device to drill a small hole in the cortical plate of the bone. The device features a hollow tubing needle (Infuser) that acts as both a drill and a hypodermic needle. During and after the drilling process, the device continuously dispenses local anesthetic into the tissue. The system is operated by a dentist in a clinical setting using a foot-pedal to control the drill motor and injection mechanism. This one-step process simplifies the traditional multi-step intraosseous injection technique, potentially improving efficiency and patient comfort during dental anesthesia administration. ## Clinical Evidence No clinical data provided; bench testing only. ## Technological Characteristics The system consists of a hollow tubing needle (Infuser) serving as both a drill and injection needle, a drill motor, and an injection motor. It is an AC-powered, hand-held device with a foot controller. The device is designed for intraosseous injection of local anesthetics. ## Regulatory Identification A spring-powered jet injector is a syringe device intended to administer a local anesthetic. The syringe is powered by a spring mechanism which provides the pressure to force the anesthetic out of the syringe. ## Predicate Devices - Stabident System - Intraosseous Local Anesthesia ([K910446](/device/K910446.md)) ## Submission Summary (Full Text) > This content was OCRed from public FDA records by [Innolitics](https://innolitics.com). If you use, quote, summarize, crawl, or train on this content, cite Innolitics at https://innolitics.com. > > Innolitics is a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices, including [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/). {0} K964802 MAY 27 1997 Appendix V Summary of Safety and Effectiveness Information 20 {1} Section 510(k) Premarket Notification Summary of Safety and Effectiveness Information Cyberjet™ Local Anesthesia System CYBERDENT, INC. Regulatory Authority: Safe Medical Devices Act of 1990, 21 CFR 807.92 1. Device Trade Name: Cyberjet™ Local Anesthesia System Common Name(s): Local Anesthesia System for Intraosseous Injection Classification Name(s): 1. Dental Injecting Needle 2. Handpiece, Direct Drive, AC-Powered 3. Injector, Jet, Mechanical-Powered 2. Establishment Name & Registration Number: Name: CYBERDENT, INC. Number: Pending 3. Classification: 1. § 872.4730 Dental injecting needle. (a) Identification. A dental injecting needle is a slender, hollow metal device with a sharp point intended to be attached to a syringe to inject local anesthetics and other drugs. (b) Classification. Class I. 2. § 872.4200 Dental handpiece and accessories. (a) Identification. A dental handpiece and accessories is an AC-powered, water-powered, air-powered, or belt-driven, hand-held device that may include a foot controller for regulation of speed and direction of rotation or a contra-angle attachment for difficult to reach areas intended to prepare dental cavities for restorations, such as fillings, and for cleaning teeth. (b) Classification. Class I. [55 FR 48439, Nov. 20, 1990] 3. § 872.4475 Spring-powered jet injector. (a) Identification. A spring-powered jet injector is a syringe device intended to administer a local anesthetic. The syringe is powered by a spring mechanism which provides the pressure to force the anesthetic out of the syringe. (b) Classification. Class II. Product Code(s): 1. 76DZM 2. 76EKX 3. 76EGH Device Class: 1. 76DZM - Class I 2. 76EKX - Class I 3. 76EGH - Class II 21 {2} # Classification Panel: 1. Dental Devices Panel 2. Dental Devices Panel 3. Dental Devices Panel ## 4. Applicant / Sponsor Name / Address: CYBERDENT, INC. 354 Bel Marin Keys, Suite I Novato, CA 94949 415.883.0484 415.883.3037 - fax ## 5. Contact Person: Mr. Gin Wu, Ph.D. CYBERDENT, INC. 354 Bel Marin Keys, Suite I Novato, CA 94949 415.883.0484 415.883.3037 - fax ## 6. Equivalent / Predicate Device(s): 1. Stabident System - Intraosseous Local Anesthesia - K910446 ## 7. Description of the Device: **Introduction.** The Cyberjet™ is a dental device intended for intraosseous injection of local anesthetics. Intraosseous injection of local anesthetics is a long-standing technique in dental anesthesia that was developed in the early 1900's and is still in common use in dental anesthesia today. Intraosseous injection requires the dentist to drill a small hole in the bone adjacent to the problem tooth. The dentist then uses a standard anesthesia needle and syringe to inject the local anesthetic solution into the previously drilled hole to numb the nerve of the tooth. The Cyberjet™ combines the dental drill and the injection needle into one device and performs both the drilling and injection functions with the same device. After an appropriate injection site has been identified, a topical anesthetic is applied to the gum, followed by a few minutes wait to allow the topical anesthetic to take effect. The previously selected injection site is located and the drill motor and the injection motor are turned on. The tip of the drill/needle is placed on the overlying gum and pressure is applied. The drill/needle passes through the soft tissue and starts to perforate the cortical plate. After the penetration of the cortical plate, the drill motor is turned off by releasing the momentary-switch on the foot-pedal. Local anesthetic is continuously dispensed into the tissue during and after the drilling process through the Infuser. Use of the Cyberjet™ will result in a simple one-step intraosseous injection for dental anesthesia. The system includes 5 components: 1. A Hollow Tubing Needle referred to as a drill/needle or Infuser that serves as a drill as well as a hypodermic injection needle. {3} DEPARTMENT OF HEALTH & HUMAN SERVICES Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAY 27 1997 Cyberdent, Incorporated C/O Mr. David W. Schlerf Buckman Company, Incorporated 1000 Burnett Avenue, Suite 450 Concord, California 94520 Re: K964802 Trade Name: Cyberjet™ Local Anesthesia System Regulatory Class: I Product Code: DZM Dated: February 26, 1997 Received: February 27, 1997 Dear Mr. Schlerf: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments, or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of {4} Page 2 - Mr. Schlerf the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or regulations. This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4692. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html". Sincerely yours, Timothy A. Ulatowski Director Division of Dental, Infection Control, and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5} Page 1 of 1 510(k) Number (if known): K964802 Device Name: CYBERIC TLOCAL ANESTHESIA SYSTEM Indications For Use: 1. Administration of intraosseous anesthesia for dental indications. PLEASE DO NOT WRITE BELOW THIS LINE - CONTINUE ON ANOTHER PAGE IF NECESSARY Concurrence of CDRH, Office of Device Evaluation (ODE) (Division Sign-Off) Susan Renner Division of Dental, Infection Control, and General Hospital Devices 510(k) Number K964802 Prescription Use ☑ (Per 21 CFR 801.109) OR Over-The-Counter Use ☐ (Optional format 1-2-96) 5 --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGM/K964802](https://fda.innolitics.com/submissions/DE/subpart-e%E2%80%94surgical-devices/EGM/K964802) **Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. 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