The FRIALIT-2® CeraBase abutment is intended for use of the following indications: Fabrication of single crowns for the anterior maxilla and mandible where exceptional esthetics are required.
Device Story
FRIALIT-2® CeraBase abutment is a two-part dental abutment system consisting of a titanium insert and an aluminum oxide ceramic sleeve. The titanium insert features a hexagonal rotational securing device that interfaces with the internal hexagon of the FRIALIT-2® implant. The ceramic sleeve is placed over the insert and secured via a slot and key connection. The device is used by dental professionals in a clinical setting to support the fabrication of single crowns. By combining a titanium base with a ceramic sleeve, the device provides a structural foundation for dental restorations while addressing esthetic requirements in the anterior region of the mouth. The color-coded titanium inserts assist the clinician in identifying appropriate diameters (3.8 mm, 4.5 mm, 5.5 mm, and 6.5 mm) to match the corresponding implant.
Clinical Evidence
Bench testing only. Comparative data provided for static shear strength (99.2 lbs vs 74.5 lbs) and dynamic fatigue strength (both runout at 35 lbs).
Technological Characteristics
Two-part abutment system. Titanium insert (ASTM F 67, Grade II) and aluminum oxide ceramic sleeve (ASTM F 603). Hexagonal rotational securing interface. Available diameters: 3.8mm, 4.5mm, 5.5mm, 6.5mm. Sterilization not specified.
Indications for Use
Indicated for patients requiring single crown restorations in the anterior maxilla and mandible where exceptional esthetics are required.
Regulatory Classification
Identification
An endosseous dental implant is a prescription device made of a material such as titanium or titanium alloy that is intended to be surgically placed in the bone of the upper or lower jaw arches to provide support for prosthetic devices, such as artificial teeth, in order to restore a patient's chewing function.
Special Controls
*Classification.* (1) Class II (special controls). The device is classified as class II if it is a root-form endosseous dental implant. The root-form endosseous dental implant is characterized by four geometrically distinct types: Basket, screw, solid cylinder, and hollow cylinder. The guidance document entitled “Class II Special Controls Guidance Document: Root-Form Endosseous Dental Implants and Endosseous Dental Implant Abutments” will serve as the special control. (See § 872.1(e) for the availability of this guidance document.)(2)
*Classification.* Class II (special controls). The device is classified as class II if it is a blade-form endosseous dental implant. The special controls for this device are:(i) The design characteristics of the device must ensure that the geometry and material composition are consistent with the intended use;
(ii) Mechanical performance (fatigue) testing under simulated physiological conditions to demonstrate maximum load (endurance limit) when the device is subjected to compressive and shear loads;
(iii) Corrosion testing under simulated physiological conditions to demonstrate corrosion potential of each metal or alloy, couple potential for an assembled dissimilar metal implant system, and corrosion rate for an assembled dissimilar metal implant system;
(iv) The device must be demonstrated to be biocompatible;
(v) Sterility testing must demonstrate the sterility of the device;
(vi) Performance testing to evaluate the compatibility of the device in a magnetic resonance (MR) environment;
(vii) Labeling must include a clear description of the technological features, how the device should be used in patients, detailed surgical protocol and restoration procedures, relevant precautions and warnings based on the clinical use of the device, and qualifications and training requirements for device users including technicians and clinicians;
(viii) Patient labeling must contain a description of how the device works, how the device is placed, how the patient needs to care for the implant, possible adverse events and how to report any complications; and
(ix) Documented clinical experience must demonstrate safe and effective use and capture any adverse events observed during clinical use.
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KG80630)
SEP 4 1998
9:46 AM ;Advanced BicResearch
# Premarket Notification 510(k) Article Name: FRIALIT-2® CeraBase Abutment
Image /page/0/Picture/4 description: The image shows a logo with a triangular shape at the top. Below the triangle, there is some text, but it is too blurry to read clearly. The logo appears to be for a company or organization, but without being able to read the text, it is difficult to determine the specific nature of the entity.
#### XI. 510(k) Summary of Safety and Effectiveness
# XI.1. Submitter Information
Submitter: Registration number: Address:
Contact Person:
Data Prepared:
Telephone:
Fax:
e-mail:
FRIATEC AG. Medical Technology Division 8681851 Stainzaugstrasse 68229 Mannheim / Germany Birgit Unger (QA/RA Manager) 011-49-621-486-1549 011-49-621-486-1856 birgit_unger@friatec.de February 2nd, 1998
XI.2. Name of Device
FRIALIT-2® CeraBase abutment Proprietary Name: Ceramic abutment for endosseous implants Common Name: Classification Name: Endosseous implants
XI.3. Predicate Device Information
| Name: | CeraOne Abutment |
|----------------|----------------------|
| Submitter: | NobelBioCare USA.Inc |
| 510(k) Number. | K961737 |
### XI.4. Description of the Device
The FRIALIT-26 CeraBase abutment is a two part abulment. It consists of the titanium insert and the caramic sleeve. The titanium insert has as the rotational securing device a hexagon. which is the counterpart to the internal hexagon of the FRIALIT-2® implant. The ceramic sleeve is blaced on top of the titanium insert where it is rotationally secured by a slot and key connection. The titanium insert is color-coded in order to clearly differentlate the different diameters.
The diameters of the FRIALIT-2® CeraBase abutments correspond to the FRIALIT-2® implant diameters. The following diameters are available:
D3,8 mm, D4,5 mm, D5,5 mm and D6,5 mm.
The FRIALIT-2® CaraBase titanium insert is manufactured out of pure titanium grade II material which is in accordance to ASTM F 67 'Standard Specification for Unalloyed Titanium for Surgical Implant Application'.
The FRIALIT-209 CeraBase ceramic sleeve is manufactured out of medical grade aluminumdioxid ceramic which Is In accordance to ASTM F 603 'Standard Specification for High-Purity Dense Aluminum Oxide for Surgical Implant Application'.
### X1.5. Intended Use
The FRIALIT-2® CeraBase abutment is intended for use of the following indications:
Fabrication of single crowns for the anterior maxilla and mandible where exceptional esthetics are required.
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: : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : : :
Premarket Notification 510(k) Artiole Name: FRIALIT-26 CeraBase Abusment
Image /page/1/Picture/3 description: The image shows a logo with a triangular shape at the top, resembling a roof or a mountain peak. Below the triangle, there is text that reads "FRIMATEC" in a stylized, slightly distressed font. The logo appears to be a simple, monochrome design, possibly representing a company or organization with a focus on construction, engineering, or a related field.
# XI.G. Technological Characteristics
The technological characteristics of the FRIALIT-20 CeraBase abutment are substantially the same as the characteristics of the NobelBioCare CeraOne abutment. Both devices consist of two single parts. One part of each is an insert or abutment made of medical grade titanium. The second part of each device is a sleeve or cap composed of aluminumdioxide ceramic. Thus, the material of construction is identical for the FRIALIT-200 CeraBase and the NobelBioCere CereOne devices (i.e. titenium and aluminumdioxide). For ratation, both devices use a hexagon that complements the internal hexegon of the implant.
The tables below show technological properties and preclinical teating results for both the FRIALIT-26 CeraBase and the predicate device.
| Properties | FRIALIT-25 CeraBase<br>abutment | NobelBioCare CeraOne<br>abutment |
|----------------------------|---------------------------------|----------------------------------|
| Al2O3 content | 99,6 weight-% | 99,0 weight-% |
| crystallogical phase | α-aluminumdioxide | α-aluminumdioxide |
| grain size parameters [µm] | d10 d50 d90<br>1,3 3,9 7,7 | d10 d50 d90<br>0,9 2,2 3,8 |
| | FRIALIT-28 ceraBase<br>abutment | NobelBioCare CeraOne<br>abutment |
|-----------------------------------|---------------------------------|----------------------------------|
| static shear strength [lbs] | 99,2 | 74,5 |
| dynamic fatigue strength<br>[lbs] | runout at 35 [lbs] | runout at 35 [lbs] |
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Image /page/2/Picture/1 description: The image shows the logo for the U.S. Department of Health & Human Services. The logo features a stylized eagle with three stripes emanating from its head, representing the department's commitment to health, human services, and well-being. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES • USA" is arranged in a circular fashion around the eagle symbol.
Food and Drug Administration 9200 Corporate Boulevard Rockville MD 20850
1 1698 SED
FRIATEC AG C/O Darcy J. Madden, M.S., M.B.A., R.A.C. Regulatory Affairs Associate Authorized Regulatory Agent for FRIATEC AG Advanced Bioresearch Associates ABA SAN DIEGO One America Plaza 600 West Broadway, Suite 900 San Diego, California 92101-3302
Re : K980630 FRIALIT-2® CeraBase Trade Name: Requlatory Class: III Product Code: DZE Dated: June 5, 1998 Received: June 8, 1998
Dear Ms. Madden:
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 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), You may, therefore, market the device, subject to the general The general controls controls provisions of the Act. provisions of the Act include requirements for annual reqistration, 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 Requlations, Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Current Good Manufacturing Practice requirements, as set forth in the Quality System Regulation (QS) for Medical Devices: General requlation (21 CFR Part 820) and that, through periodic QS inspections, the Food and Drug Failure to Administration (FDA) will verify such assumptions.
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Page 2 - Ms. Madden
comply with the GMP regulation may result in regulatory In addition, FDA may publish further announcements action. 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 the Act for devices under the Electronic Product Radiation Control provisions, or other Federal laws or requlations.
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 requlation (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" (21CFR 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.qov/cdrh/dsma/dsmamain.html".
Sincerely yours,
A. Butman for
Timothy A. Ulatowski Director Division of Dental, Infection Control, -and General Hospital Devices Office of Device Evaluation Center for Devices and Radiological Health
Enclosure
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Page of
510(k) Number (if known)
Device Name:__FRIALIT-2(r) CeraBase
Indications For Use:
The FRIALIT-2(t) CetaBase abutment is intended The FRIALIT-2(t) Cerabase aon theme to rowns for "
for use in the fabrication of single crowns for for use in the fabrication of original and exceptional esthetics are required.
(PLEASE DO NOT WRITE BELOW THIS LINE-CONTINUE ON ANOTHER PAGE IF NEEDED)
Concurrence of CDRH, Office of Device Evaluation (ODE)
Prescription Use
(Per 21 CFR 801:109)
OR
Over-The-Counter Use
(Optional Format 1-2-96)
Susan Pun
(Division Sign-Off)
Division of Dental, Infection Control,
and General Hospital Devices
510(k) Number 1980630
Two short videos show you everything — or skip straight to the written tutorial if you'd rather read. You can reopen this any time from the Tutorial button in the top bar.
Part 1 — Search, results, and everyday workflows 16 min
Part 2 — Embeddings: the galaxy map 3 min
1. Search: exact and fuzzy
Type a phrase like "coronary artery calcification" into the search box. You get two kinds of results. Exact results match the literal phrase — prefix searches work ("coronary artery calcificati") but suffix searches do not. Fuzzy results match on the meaning and intent of your phrase rather than the exact words, and are sorted by relevance score. Hover over the Exact or Fuzzy badge on any row to see exactly why it matched.
Use the checkboxes above the results to narrow: SaMD keeps only software-only devices, AI / ML keeps only devices with AI.
Exact vs. fuzzy search: what's the difference?
Exact matches on the literal phrase (prefix search works, suffix does not). Fuzzy matches on the meaning and intent of the phrase rather than the exact words. Hover over the badge on any row to see why it matched.
You search "coronary artery calcification" and want only software devices with AI. What two filters do you apply?
Narrow by SaMD (software-only devices), then narrow by AI/ML (devices with AI).
2. The results table
Scroll right in the results table. The intended use is extracted for you — no need to open the PDF. The device story gives a high-level snapshot of what the device does and how it's used. The AI Performance sub-table shows each output name, acceptance criteria, observed values, and development/test dataset descriptions — the same format Innolitics uses for regulatory strategy outputs, and the fastest high-level fingerprint of an AI device. It is AI-generated but has been very reliable in practice.
Where do you find a device's intended use without opening the PDF?
Scroll right in the search results table. The intended use column is extracted for you; no need to dig into the 510(k) summary PDF.
What does the AI Performance sub-table show, and why is it useful?
Output name, acceptance criteria, observed values, development dataset description, and test dataset description. It's the same format we use for regulatory strategy output and Fast 510(k) input, and the fastest high-level fingerprint of an AI device. AI-generated but reliable in practice.
3. Judging fuzzy relevance
Fuzzy results trail off in relevance as you scroll. Use three signals to decide how far down to go: the fuzzy badge explanations, the intended use column, and whether your target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, you're past the relevant zone. A top hit with a low score (~0.4) and a stretched explanation is a hint the closest predicates are far away — the project may be headed for De Novo. Note the fuzzy search is a pattern match: it doesn't handle negation ("not") well, and hardware devices can appear — filter by SaMD/AI ML to cut them.
How do you judge how far down fuzzy search results to go?
Use the relevancy signals: the fuzzy badge explanations, the intended use column, and whether the target output (e.g., Cobb angle) still appears in the AI Performance sub-table. Once it stops appearing, results are trailing off in relevancy.
4. Device detail page: chat and citations
Click a device name to open its detail page: device facts on the left, a chat window on the right. Ask something like "Describe the training data". The answer carries little citation bubbles — click one to jump to the highlighted passage in the source PDF, so you can verify every AI answer against the document. There's also a Download PDF button for sharing.
How do you verify an AI chat answer on the device detail page?
Click the citation bubbles to jump to the relevant highlight in the source document.
Reading rule for every project: how many summaries do you read in full?
At least the three most relevant 510(k) or De Novo summaries, in full. After that, use targeted chat questions to confirm your memory quickly. The tool supports this professional habit — it doesn't replace it.
5. Side-by-side comparison
Select multiple rows in the results table (aim for under ~10), then open the PDF Viewer tab. Ask one question — it goes to all selected devices in parallel, each with citations. This is the fastest way to compare and contrast devices: training data, PCCP scope, how they handled adding new scanners, and so on.
What does the side-by-side PDF viewer mode do?
Select multiple devices, open the PDF viewer tab, and ask one question (e.g., "Describe the training data"). It queries all selected devices simultaneously with citations, so you can compare and contrast quickly.
6. Collections
With rows selected, go to the Collections tab and create a labeled collection (e.g., "Cobb Angle Project"). Reload that selection any time — before a client call, pull up the collection and ask questions across all of its devices at once.
How do you save a set of selected devices for later use?
Select the rows, go to the Collections tab, and create a labeled collection (e.g., "Cobb Angle Project"). You can reload the selection anytime and carry it into the PDF viewer and other tabs that support selections.
7. Product codes and the regulations tree
Click a product code in the results to jump to it in the regulations tree — identification text, sibling product codes, and devices you can open in a PDF viewer on the right. Click a regulation number to see its identification, special controls, and related product codes. You can also search by product code or regulation number at the top of the tree. Always read the special controls if any exist for your device — it broadens your search and sharpens pre-kickoff research.
What can you do from the regulations tree view?
Browse product codes and regulation numbers, read the identification text and special controls, browse sibling product codes, open device PDFs on the right, and search by product code or regulation number at the top of the tree.
8. Chart view
Click Show Chart and segment by regulation number (or product code) to see which regulations dominate your result set. Clicking a regulation takes you into the regulations tree. Great for spotting that most matches are, say, hardware laparoscopic devices — a cue to go back and filter.
How do you see which regulations dominate a search result set?
Click "Show Chart" and segment by Regulation Number. Clicking a regulation takes you to the regulations tree.
9. The predicate graph
Open the Predicates tab for a family-tree view of predicate relationships. Click a node to trace its parents and children; selections from search carry over pre-selected. Commonly predicated devices are worth reading — a lot of people predicated them for a reason. The visual lineage is also handy on client calls, e.g. to show how a predicate family evolved and justify why your predicate still holds.
In the predicate graph, why are commonly predicated devices worth reading?
A lot of people predicated them for a reason. Clicking a node traces parents and children, and selections from search carry over pre-selected.
10. Embeddings: the galaxy map
The Embeddings tab plots every matching document in a 2-D "galaxy map" where semantically similar devices cluster together. Hover or click clusters to explore, and let AI label the clusters for you. Embeddings beat product codes for grouping: two devices can carry different product codes (LLZ vs. QIH) yet do the same thing — the embedding captures the meaning of the intended use and device story. This is also exactly how retrieval-augmented generation (RAG) works under the hood, and it makes a great visual on client calls.
Try it yourself
Head to the search page and work through a few of these AI/ML fuzzy searches to build intuition: perivascular fat on CT · aortic valve calcification opportunistic screening on noncontrast CT · breast cancer prediction on digital pathology slides · autism detection · gestational age prediction · a hearing aid that can also detect a pulse · foundation model based analysis of ECG · large language models · penetration test. Watch how the relevance scores, intended use, and AI Performance tables tell you when results stop being meaningful.
