← Product Code [EJT](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJT) · K024143 # AIGIS-FINE (K024143) _Sb Lucius, Inc. · EJT · Mar 10, 2003 · Dental · SESE_ **Canonical URL:** https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJT/K024143 ## Device Facts - **Applicant:** Sb Lucius, Inc. - **Product Code:** [EJT](/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJT.md) - **Decision Date:** Mar 10, 2003 - **Decision:** SESE - **Submission Type:** Traditional - **Regulation:** 21 CFR 872.3060 - **Device Class:** Class 2 - **Review Panel:** Dental - **Attributes:** Therapeutic ## Indications for Use AIGIS-FINE is intended for manufacturing - Inlay / Onlays - - Crowns - - Short span bridges - - Long span bridges - - Removable partials - ## Device Story AIGIS-FINE is a gold-based dental casting alloy used by dental professionals for the fabrication of restorative dental prosthetics. The alloy is melted and cast to form inlays, onlays, crowns, and bridges. It serves as a restorative material to replace missing or damaged tooth structure, providing structural support and functional restoration for patients requiring dental prostheses. The device is utilized in a dental laboratory or clinical setting by dental technicians or dentists. ## Clinical Evidence Bench testing only. Physical and mechanical properties (melting point, Vickers hardness, yield strength, elongation, and density) were compared against the predicate device. Testing methods applied were in accordance with ANSI/ADA 5 and ISO 9693. ## Technological Characteristics Gold-based dental casting alloy. Melting point range: 1,730-1,832 °F; Vickers hardness: 145; Yield strength: 250 MPa; Elongation: 26%; Density: 15.19 g/cm3. Tested per ANSI/ADA 5 and ISO 9693 standards. ## Regulatory Identification A noble metal alloy is a device composed primarily of noble metals, such as gold, palladium, platinum, or silver, that is intended for use in the fabrication of cast or porcelain-fused-to-metal crown and bridge restorations. ## Special Controls *Classification.* Class II (special controls). The special control for these devices is FDA's “Class II Special Controls Guidance Document: Dental Noble Metal Alloys.” The devices are exempt from the premarket notification procedures in subpart E of part 807 of this chapter subject to the limitations in § 872.9. See § 872.1(e) for availability of guidance information. ## Predicate Devices - AUROFLUID M ([K993475](/device/K993475.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}------------------------------------------------ K024143 # MAR 1 0 2003 ## 510(K) SUMMARY SB LUCIUS, INC. Submitter of 510(k): 9778 Katella Ave. Ste. 205, Anaheim, CA 92804 Phone: (714) 530-2814, Fax : (714) 530-3448, | Contact person: | Dae Kyu Chang | |-----------------|---------------------| | Phone: | (714) 530-2814 | | Fax: | (714) 530-3448 | | E-mail: | Gatorkr@yahoo.co.kr | Date of Summary: Dec 15, 2002 Trade name: Common: Classification name: AIGIS-FINE Dental casting alloy Gold based alloys and precious metal alloys for clinical use EJT Class II Froduct code: Classification: Legally marketed device: AUROFLUID M 510(k) number: K993475 ## SUMMARY OF THE TECHNOLOGICAL CHARACTERISTICS Test methods applied: as in ANSI/ADA 5 and ISO 9693 Comparison of composition: | | ' אורון זו וכיו
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- | | | and the program montan and any and other the commended | | ------------------------------------------------------------------------------------------------------------------------------------------------------------------------------ | | # POSITION (WEIGHT %) #### Comparison of physical and mechanical properties: | Alloy | Melting Point Range (°F) | Hardness (Vickers) | Yield Strength (MPa) | Elongation (%) | Density (g/cm3) | |-------------|--------------------------|--------------------|----------------------|----------------|-----------------| | AUROFLUID M | 1,687-1,777 | 155 | 340 | 27 | 15.4 | | AIGIS-FINE | 1,730-1,832 | 145 | 250 | 26 | 15.19 | {1}------------------------------------------------ ## Discussion: 'Since the composition of the legally marketed alloy and the new device is very similar, it may be assumed that the biological compatibility of the alloys is also very similar. ### Conclusion: The main elements and their concentration are almost identical. AIGIS-FINE is an inlay, onlay, crown and bridge alloy. This device is dependable 7 1% gold alloy with a high gold appearance. AIGIS-FINE is excellent for inlays, three-quarter crowns, long and short-span bridges. AIGIS-FINE is substantially equivalent to Metalor's AUROFLUID M and the minor d fferences between them do not affect safety or effectiveness. {2}------------------------------------------------ Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo is circular and contains the words "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" around the perimeter. Inside the circle is a stylized image of three human profiles facing right, with flowing lines connecting them. The logo is black and white. MAR 1 0 2003 Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850 Mr. Dae-Kyu Chang SB LUCIUS. Incorporated 9778 Katella Avenue, Suite 205 Anaheim, California 92804 Re: K024143 Trade/Device Name: AIGIS-Fine Regulation Number: 872.3060 Regulation Name: Gold-based Alloys and Precious Metal Alloys for Clinical Use Regulatory Class: II Product Code: EJT Dated: December 15, 2002 Received: December 16, 2002 Dear Mr. Chang 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 indications for 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 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 (PMA). it may be subject to such additional controls. Existing major regulations affecting vour 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 Federal Register. {3}------------------------------------------------ Page 2 - Mr. Chang Please be advised that FDA's issuance of a substantial equivalence determination does not mean that FDA has made a determination that your device complies with other requirements of the Act or any Federal statutes and regulations administered by other Federal agencies. You must comply with all the Act's requirements, including, but not limited to: registration and listing (21 CFR Part 807); labeling (21 CFR Part 801); good manufacturing practice requirements as set forth in the quality systems (QS) regulation (21 CFR Part 820); and if applicable, the electronic product radiation control provisions (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) 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). please contact the Office of Compliance at (301) 594-4613. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21CFR Part 807.97). You may obtain other general information on your responsibilities under the Act from the Division of Small Manufacturers, International and Consumer Assistance at its toll-free number (800) 638-2041 or (301) 443-6597 or at its Internet address http://www.fda.gov/cdrh/dsma/dsmamain.html Sincerely yours, Susan Purser Susan Runner, DDS, MA Interim Director Division of Anesthesiology, General Hospital, Infection Control and Dental Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {4}------------------------------------------------ SB LUCIUS,INC. 9778 Katella Ave. Ste. 205, Anaheim, CA 92804 Phone: (714) 530-2814, Fax : (714) 530-3448, # INDICATIONS FOR USE 510(K) Number : ______________________________________________________________________________________________________________________________________________________________ Device Name(s) : AIGIS-FINE AIGIS-FINE is intended for manufacturing - Inlay / Onlays - - Crowns - - Short span bridges - - Long span bridges - - Removable partials - (PLEASE DO NOT WRITE BELOW THIS LINE CONTINUE ON ANOTHER PAGE IF NEEDED) ============================================================================================================================================================================== concurrence of chrd,office of device evaluation(oed) Mccarthy for MSR esiology. General Hospital. 510(k) Number: --- **Source:** [https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJT/K024143](https://fda.innolitics.com/submissions/DE/subpart-d%E2%80%94prosthetic-devices/EJT/K024143) **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. If you're preparing [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/), [get in touch](https://innolitics.com/contact). **Cite:** Innolitics at https://innolitics.com