Who is the manufacturer of AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV?

J. Morita USA, Inc. filed the 510(k) submission for AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV (K043497).

What is the FDA product code for AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV?

EFB. It is classified under 21 CFR 872.4200 as a Class 1 device in the Dental panel.

What is the regulatory pathway for AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV?

510(k) clearance (submission type: Traditional).

What are the predicate devices for AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV?

Siroair L air scaler (K033812).

Who can help prepare an FDA 510(k) submission like AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV?

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV

K043497 · J. Morita USA, Inc. · EFB · Mar 21, 2005 · Dental

Device Facts

Record ID	K043497
Device Name	AIR SOLFY, MODELS AS-4H, AS-4H-O, AS-4H-V, AS-4H-OV, AS-1,AS-1-0,AS-1-V, AS-1-OV
Applicant	J. Morita USA, Inc.
Product Code	EFB · Dental
Decision Date	Mar 21, 2005
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 872.4200
Device Class	Class 1
Attributes	Therapeutic

Intended Use

The Air Solfy can be used to remove calculus deposits from teeth by application of an air-powered vibrating scaler tip from the teeth during dental cleaning and periodontal therapy.

Device Story

Air Solfy is an air-powered dental handpiece scaler used for removing calculus deposits during dental cleaning and periodontal therapy. The device connects to a dental unit, receiving air for the high-speed air turbine, cooling water for the scaling site, and an optional light source for illumination. It operates by converting air energy into mechanical vibration of a scaler tip, which is applied to the tooth surface. Cooling water is delivered through pouring holes to the treatment area. The device is used in a clinical dental setting by a dentist or dental hygienist. It is available in various configurations, including options for integrated light and power adjustment, and is designed to be autoclavable. The output is the mechanical vibration of the tip, which facilitates the physical removal of calculus, aiding in periodontal health.

Clinical Evidence

No clinical data provided. Substantial equivalence is based on bench testing and compliance with international standard ISO 15606:1999.

Technological Characteristics

Air-powered dental handpiece; energy source: compressed air from dental unit; cooling water delivery system; optional integrated light source; optional power adjuster; autoclavable; compliant with ISO 15606:1999; connection types include MORITA original joint or ISO 9168 type C coupling.

Indications for Use

Indicated for removal of calculus deposits from teeth during dental cleaning and periodontal therapy. For use by dental professionals.

Regulatory Classification

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.

Predicate Devices

Siroair L air scaler (K033812)

Related Devices

K033812 — SIROAIR L AIR SCALER · Sirona Dental Systems GmbH · Feb 23, 2004
K161639 — Y-MIC · Micron Corporation · Dec 22, 2016
K991021 — SONIC SCALER WITH FIBER OPTIC, MODEL NAS-L, SONIC SCALER WITHOUT FIBER OPTIC, MODEL NAS-NL · Nsk Nakanishi, Inc. · Jun 23, 1999
K083059 — AIR SONIC SCALER · Dpm USA Corp. · Jan 30, 2009
K964596 — PROSELECT 3 PERIDONTAL THERAPY SYSTEM · Professional Dental Mfg., Inc. · Apr 22, 1997

Submission Summary (Full Text)

{0}------------------------------------------------ K043497 #### 510(k) SUMMARY ### J. MORITA MFG. CORP.'s Air Solfy # Name of Device and Name/Address of Sponsor | Trade or Proprietary Name: | Air Solfy AS series (AS-4H/ AS-4H-O/ AS-4H-V/ AS-4H-OV and AS-1/ AS-1-O/ AS-1-V/ AS-1-OV) | |----------------------------|-------------------------------------------------------------------------------------------------| | Common Name: | Dental scaler | | Classification Name: | Dental Handpiece and accessories (21CFR872.4200) | | Product Code : | EFB ("Handpiece, Air-powered, Dental) | | Registration No. 2081055 | Registration No. 3002807636 | | Initial Distributor: | Manufacturer: | |----------------------|----------------------------| | J. Morita USA, Inc. | J. MORITA MFG. CORP. | | 9 Mason | 680 Higashihama Minami-cho | | Irvine, CA 92618 | Fushimi-ku, Kyoto | | USA | Japan 612-8533 | | Telephone: | 949-581-9600 | | | +81-75-611-2141 | | Facsimile: | 949-581-9688 | | | +81-75-605-2354 | #### Intended Use . The Air Solfy can be used to remove calculus deposits from teeth by application of an air-powered vibrating scaler tip from the teeth during dental cleaning and periodontal therapy. ## Technological Characteristics and Substantial Equivalence This device receives energy resorces in handpiece such as air for high speed air turbine, cooling water for scaling and light source for illumination, through the tubes connected to a dental unit. The cooling water is fed on the part of scaling treatment through pouring holes. Air Solfy is classified into the model as is shown below Table-1 from the variations of connection, light or power adjuster. {1}------------------------------------------------ | ml: 1 1 | € 1 1 | | |---------------|-------------|--| | | | | | Table-1 | Model of Air Solfy | |---------|--------------------| |---------|--------------------| | | | | ( - : not included ) | | |-----------|------------------|----------|----------------------|--------------| | Model | Connection | Light | Power Adjuster | Autoclave | | AS-1 | They can be | - | - | | | AS-1-O | connected to the | Included | - | Autoclavable | | AS-1 V | MORITA original | - | Included | | | AS-1-O V | a joint. | Included | Included | | | AS-4H | They can be | - | - | | | AS-4H-O | connected to the | Included | - | Autoclavable | | AS-4H V | CP4 or CP4-O | - | Included | | | AS-4H-O V | coupling. NOTE-1 | Included | Included | | NOTE-1 CP4 or CP4-O is the ISO9168 type C coupling. Air Solfy covered by this submission is substantially equivalent to other legally marketed device. Specifically, Air Solfy is substantially equivalent to the Siroair L air marketed do from Sirona dental syatem , Inc(K#033812). Air Solfy has similar general seater "from Birona contraciples of operation, and similar technological characteristics as the previously cleared predicate device, Siroair L air scaler. Although we cannot compare specifications of them minutely as we have not obtained Andrough Tre Sailfor sons of Siroair L, but we are able to figure out the specifications und equivalence as there exists a common international standard on the dental airand equivaliere of ISO 15606. Air Solfy is in compliance with ISO 15606:1999. The Air Solfy's substantial equivalence to Siroair L is demonstrated at Comparison Summary Table as below. Although there are minor differences in the characteristics of Air Solfy and its predicate device, these differences do not raise new questions of safety or effectiveness. {2}------------------------------------------------ | FDA file reference number | 510k number K033812 | |-----------------------------------------------------|------------------------| | Attachment inside notification submission file | 510k FDA | | TECHNOLOGICAL CHARACTERISTICS | Comparison result | | Indication for use | Identical | | Target population | Identical | | Design | Similar | | Materials | Similar | | Performance | Similar | | Sterility | Similar | | Biocompatibility | Similar | | Mechanical safety | Similar | | Chemical safety | Similar | | Anatomical sites | Similar | | Human factors | Similar | | Energy used and/or delivered | Similar | | Compatibility with environment and other devices | Similar | | Where used | Identical | | Standards met | Similar | | Electrical safety | Similar | | Thermal safety | Not applicable | | Radiation safety | Not applicable | ## Substantial Equivalent comparison table {3}------------------------------------------------ DEPARTMENT OF HEALTH & HUMAN SERVICES Image /page/3/Picture/1 description: The image shows the logo for the Department of Health and Human Services, USA. The logo consists of a stylized caduceus symbol, which is a staff with a serpent entwined around it, representing medicine and health. The text "DEPARTMENT OF HEALTH AND HUMAN SERVICES, USA" is arranged in a circular fashion around the symbol. Public Health Service Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 MAR 2 1 2005 J. Morita USA, Incorporated C/O Mr. Keith A. Barritt Fish & Richardson P.C. 1425 K Street, N.W. 11th Floor Washington, DC 20005 Re: K043497 Ro43477 Trade/Device Name: Air Solfy Air Powered Dental Handpiece Scaler and Tips Regulation Number: 872.4200 Regulation Name: Dental Handpiece and Accessories Regulatory Class: I Product Code: EFB Dated: March 3, 2005 Received: March 4, 2005 Dear Mr. Barritt: We have reviewed your Section 510(k) premarket notification of intent to market the device referenced above and have determined the device is substantially equivalent (for the included a or use stated in the enclosure) to legally marketed predicate 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) that do not require approval of a premarket approval application (PMA). You may, therefore, market the device, subject to the general approvisions 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 (PMA), 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 898. In addition, FDA may publish further announcements concerning your device in the Eederal Register. {4}------------------------------------------------ #### Page 2 - Mr. Barritt Please be advised that FDA's issuance of a substantial equivalence determination does not Please be advised that I DA 3 issualled of a basean and many of the with other requirements mean that I DA has made a determinations administered by other Federal agencies. of the Act of ally I edelar statues and registered. You must comply with all the Act s requirements, including, but not limited to: registration 1 out must comply with an any labeling (21 CFR Part 801); good manufacturing practice and listing (21 CFR Patt 607), labeling (21 CFR Part 820); and if requirents as set forth in the quality byocans (Sections 531-542 of the Act); 21 CFR 1000-1050. This letter will allow you to begin marketing your device as described in your Section 510(k) I mis letter will anow you to begin maliering of substantial equivalence of your device to a premiarket notification. THE I D. I mails 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), IT you desire specific advice for Jour at (240) 276-0115. Also, please note the regulation in prease contact the Other or Somphise or premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the may obtain other general miernational and Consumer Assistance at its toll-free Driston 01 01 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/industry/support/index.html. Sincerely yours, Susan Runne Chiu Lin, Ph.D. Chiu Lin, Ph.D. Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {5}------------------------------------------------ # Indications for Use 510(k) Number (if known): K043497 AIR SOLFY AIR POWERED DENTAL HANDPIECE SCALER AND TIPS Device Name: Indications For Use: The Air Solfy is a dental air-powered handpiece scaler and tips that can remove calculus deposits from the teeth by application of an air-powered vibrating scaler tip to the teeth during dental cleaning and periodontal therapy. Prescription Use _ X (Part 21 CFR 801 Subpart D) AND/OR Over-The-Counter Use (21 CFR 801 Subpart C) (PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED) Concurrence of CDRH, Office of Device Evaluation (ODE) Susan Ruane 11 0. 201 ; (2010) Par Page 1 of 1