510(k) · Cleared

Cleared

Carbon Fiber Bridge, Model 28757

K031070510(k) TraditionalCleared Jul 3, 200390-day reviewClass II21 CFR 872.3760

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Nobel Biocare AB · EBI Resin, Denture, Relining, Repairing, Rebasing

Cleared on Jul 3, 2003 as substantially equivalent to K013881 (Ribbond, Inc., 2002) and 2 other predicates after a 90-day review. Its family tree reaches back 2 generations to 2001.

Decided: Jul 3, 2003
Review: 90 days
Class: Class II
Product code: EBI
Recalls: None
Predicates: 3

Its longest line of descent runs back 2 generations to K003333 (2001). 4 ancestors in all, the oldest K913040 (1991). No later device cites it as a predicate yet.

By dateBy generation

Root · 2 generations backK003333 STICKStick Tech, Ltd. · 2001
1 generation backK011788 EverstickStick Tech, Ltd. · 2001
This deviceK031070 Carbon Fiber Bridge, Model 28757Nobel Biocare AB · 2003

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−2	K003333	STICK	Stick Tech, Ltd.	2001	—
−1	K011788	Everstick	Stick Tech, Ltd.	2001	—
0 (this device)	K031070	Carbon Fiber Bridge, Model 28757	Nobel Biocare AB	2003	—

Other ancestors by year cleared

Year cleared	Devices	With a Class I recall
1991	1	0
2002	1	0

FIG. 1 — Lineage of K031070, 2001–2003Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in EBI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new EBI device

#1 K250617 Apex Flexscore 18.3 · 1 generation · no Class I recall
#2 Held for the reportin the report
#3 Held for the reportin the report

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What was it cleared against? (3)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

Type	Number	Device	Applicant	Decided	Recalls
*	K013881	Ribbond - Triaxial Summary page 1 …ng Resin (21 CFR 872.3760) Trade or Proprietary or Model Name: Carbon Fiber Bridge Legally Marketed Device(s): Ribbond - Triaxial (K013881) EverstickTM(KO1 1788) StickTM(K003333) Device…	Ribbond, Inc.	2002	—
*	K011788	Everstick	Stick Tech, Ltd.	2001	—
*	K003333	STICK Summary page 1 …arketed Device(s): Ribbond - Triaxial (K013881) EverstickTM(KO1 1788) StickTM(K003333) Device Description: The Carbon Fiber Bridge provides an alternative to traditional gold/metal framework in the creation of de…	Stick Tech, Ltd.	2001	—

Also cleared against K013881: 1 other device →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

The line of descent spans 2 years and passes through 2 companies; a new generation was cleared every 1.7 years on median.
None of the 4 ancestors has a recall.
1 other device also cites its predicate K013881.

How does its category compare?

All EBI devices

EBI Resin, Denture, Relining, Repairing, Rebasing: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · EBI

11in 2025

2007high 11 (2011) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EBI

79in 2025

2007high 283 (2020) · low 53 (2007)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · EBI

2in 2022

2007high 2 (2018) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · EBI

34in 2025

2007high 34 (2025) · low 1 (2024)2025

MAUDE reports naming product code EBI, not matched to any one device; reports are not rates.

View these four charts as a table

Year	Decisions	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	10	53	0	7
2008	6	124	0	2
2009	3	234	0	5
2010	4	95	0	4
2011	11	113	0	6
2012	3	85	0	9
2013	5	135	0	5
2014	5	102	0	9
2015	9	106	0	8
2016	7	147	0	9
2017	8	196	0	2
2018	5	158	2	2
2019	4	127	0	10
2020	6	283	0	8
2021	4	99	0	25
2022	11	154	2	2
2023	11	96	0	13
2024	9	90	0	1
2025	11	79	0	34
2026	7	87	0	—

What is it indicated for?

The Carbon Fiber Bridge is indicated for use as a denture base material providing reinforcement of prosthetic reconstructions in the treatment of fully or partially edentulous patients in order to restore the patient’s chewing function.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K031070 · printed Nov 6, 2026

Cite this page

510(k) Report. “K031070: Carbon Fiber Bridge, Model 28757.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K031070

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Record history

FDA decision record loaded May 2, 2026
Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
Lineage and recalls computed Nov 3, 2026
Page last updated Nov 3, 2026