510(k) · Cleared

Cleared

Proximerge 2 Dental Implant System

K211409510(k) TraditionalCleared Oct 19, 2022531-day reviewClass II21 CFR 872.3640

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

Quadric Biomed, LLC · DZE Implant, Endosseous, Root-Form

Cleared on Oct 19, 2022 as substantially equivalent to K092035 (Bicon, LLC, 2009) after a 531-day review. Its family tree reaches back 1 generation to 2009.

Decided: Oct 19, 2022
Review: 531 days
Class: Class II
Product code: DZE
Recalls: None
Predicates: 1

Its longest line of descent runs back 1 generation to K092035 (2009). No later device cites it as a predicate yet.

By dateBy generation

Root · 1 generation backK092035 Bicon Implants with a 2.5MM Internal ConnectionBicon, LLC · 2009
This deviceK211409 Proximerge 2 Dental Implant SystemQuadric Biomed, LLC · 2022

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
−1	K092035	Bicon Implants with a 2.5MM Internal Connection	Bicon, LLC	2009	—
0 (this device)	K211409	Proximerge 2 Dental Implant System	Quadric Biomed, LLC	2022	—

FIG. 1 — Lineage of K211409, 2009–2022Source: 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 DZE? 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 DZE device

#1 K211090 ZENEX Implant Systemscore 25.4 · 15 generations · 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? (1)

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
*	K092035	Bicon Implants with a 2.5MM Internal Connection Summary page 4 …n principles to the following predicate and reference devices: 510k Number Trade or Proprietary or Model Name Manufacturer Predicate Type K092035 Bicon Implants with a 2.5mm Internal Connection Bicon, LLC Primary Predicate K972417 6.0 x 8.0mm D…	Bicon, LLC	2009	—
†	K972417	The 6.0 X 8.0MM Dental Implant System	Bicon, Inc.	1997	—
†	K171784	Straumann Dental Implant System	Straumann USA, LLC	2018	—
†	K201334	Keystone Dental XL Dental Implant System	Keystone Dental, Inc.	2020	—

Also cleared against K092035: 13 other devices →

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?

Its one ancestor has no recall.
13 other devices also cite its predicate K092035.

How does its category compare?

All DZE devices

DZE Implant, Endosseous, Root-Form: FDA decisions, review times, recalls and adverse event reports over 20 years. 2022, this device’s year, is highlighted.

FDA decisions per year · DZE

31in 2025

2007high 61 (2008) · low 26 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DZE

184in 2025

2007high 265 (2014) · low 107 (2007)2026

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

Recalls per year · DZE

1in 2025

2007high 15 (2016) · low 0 (2011)2026

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

Adverse event reports per year · DZE

465,788in 2025

2007high 537,585 (2023) · low 164 (2009)2025

MAUDE reports naming product code DZE, 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	43	107	11	225
2008	61	118	4	393
2009	41	110	3	164
2010	34	162	3	360
2011	26	194	0	362
2012	39	174	11	358
2013	42	195	1	391
2014	36	265	7	1,124
2015	36	215	3	2,894
2016	40	219	15	1,116
2017	48	223	4	9,719
2018	41	200	4	12,892
2019	31	231	8	167,016
2020	41	230	0	255,524
2021	34	182	6	479,618
2022	34	243	0	483,224
2023	35	248	0	537,585
2024	40	222	1	473,629
2025	31	184	1	465,788
2026	15	194	2	—

What is it indicated for?

The Proximerge™ 2 Dental Implant System is designed for use in edentulous sites in the mandible or maxilla as a single tooth replacement. These implants are indicated for delayed loading.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K211409 · printed Nov 3, 2026

Cite this page

510(k) Report. “K211409: Proximerge 2 Dental Implant System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K211409

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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