510(k) · Cleared

Cleared

Camlog Implant System Abutments

K073553510(k) TraditionalCleared Mar 5, 200878-day reviewClass II21 CFR 872.3630

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

Altatec GmbH · NHA Abutment, Implant, Dental, Endosseous

Cleared on Mar 5, 2008 after a 78-day review. The FDA summary names no predicate by number. 85 later devices descend from it.

Decided: Mar 5, 2008
Review: 78 days
Class: Class II
Product code: NHA
Recalls: None
Predicates: 0

85 later devices descend from it, 4 citing it directly.

This deviceK073553 Camlog Implant System AbutmentsAltatec GmbH · 2008
Descendant · cites it directly · 83 of its ownK102804 Spi Titanium Base for Cad/CamThommen Medical AG · 2011
Descendant · cites it directly · 45 of its ownK103691 Biohorizons Abutments for ZimmerBioHorizons Implant Systems, Inc. · 2011 · Recalled
Descendant · 2 generations on · 36 of its ownK112440 AB Dental Devices Implants and AccessoriesA.B. Dental Devices, Ltd. · 2012
Descendant · cites it directly · 30 of its ownK103291 Biohorizons Laser-Lok Abutments for Nobel BiocareBioHorizons Implant Systems, Inc. · 2011
Descendant · 2 generations on · 29 of its ownK122295 Core 3D Abutment System for Digital Prosthetic SolutionsCore 3D Protech, S.L. · 2013

Showing 5 of 85 descendants. See all descendants

Descendants cleared per year

2011high 9 (2022) · low 2 (2012)2026

Most influential descendants

Showing 5 of 85 · See all

K102804Spi Titanium Base for Cad/CamThommen Medical AG · 2011 · cites it directly83descendants
K103691Biohorizons Abutments for ZimmerBioHorizons Implant Systems, Inc. · 2011 · cites it directly45descendants
K112440AB Dental Devices Implants and AccessoriesA.B. Dental Devices, Ltd. · 2012 · 2 generations on36descendants
K103291Biohorizons Laser-Lok Abutments for Nobel BiocareBioHorizons Implant Systems, Inc. · 2011 · cites it directly30descendants
K122295Core 3D Abutment System for Digital Prosthetic SolutionsCore 3D Protech, S.L. · 2013 · 2 generations on29descendants

View FIG. 1 as a table

Line of descent and top descendants

Generation	Number	Device	Applicant	Decided	Recalls
0 (this device)	K073553	Camlog Implant System Abutments	Altatec GmbH	2008	—
+1	K102804	Spi Titanium Base for Cad/Cam	Thommen Medical AG	2011	—
+1	K103691	Biohorizons Abutments for Zimmer	BioHorizons Implant Systems, Inc.	2011	1
+2	K112440	AB Dental Devices Implants and Accessories	A.B. Dental Devices, Ltd.	2012	—
+1	K103291	Biohorizons Laser-Lok Abutments for Nobel Biocare	BioHorizons Implant Systems, Inc.	2011	—
+2	K122295	Core 3D Abutment System for Digital Prosthetic Solutions	Core 3D Protech, S.L.	2013	—

Descendants by year cleared

Year cleared	Devices	With a Class I recall
2011	3	0
2012	2	0
2013	2	0
2014	4	0
2015	2	0
2016	7	0
2017	4	0
2018	3	0
2019	5	0
2020	8	0
2021	6	0
2022	9	0
2023	8	0
2024	8	0
2025	9	0
2026	5	0

FIG. 1 — Lineage of K073553, 2008–2026Source: 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 NHA? 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 NHA device

#1 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 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?

The FDA summary names no predicate by number.

What descends from it? (85)

See all 85

4 later devices cite it directly; ranked here by how many devices descend from each in turn.

Number	Device	Applicant	Decided	Descendants
K102804	Spi Titanium Base for Cad/Cam	Thommen Medical AG	2011	83
K103691	Biohorizons Abutments for Zimmer	BioHorizons Implant Systems, Inc.	2011	45
K103291	Biohorizons Laser-Lok Abutments for Nobel Biocare	BioHorizons Implant Systems, Inc.	2011	30
K121391	Inclusive Titanium Abutments for Camlog Screw-Line Implants	Prismatik Dentalcraft, Inc.	2012	0

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?

Of its descendants, K102804 (Thommen Medical AG, 2011) has gone furthest, with 83 descendants of its own.

How does its category compare?

All NHA devices

NHA Abutment, Implant, Dental, Endosseous: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · NHA

40in 2025

2007high 51 (2023) · low 19 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHA

147in 2025

2007high 211 (2021) · low 90 (2008)2026

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

Recalls per year · NHA

1in 2025

2007high 36 (2016) · low 0 (2009)2026

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

Adverse event reports per year · NHA

838in 2025

2007high 858 (2015) · low 1 (2007)2025

MAUDE reports naming product code NHA, 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	38	91	1	1
2008	31	90	2	8
2009	30	95	0	30
2010	19	162	0	61
2011	31	130	5	56
2012	25	171	1	5
2013	22	184	1	143
2014	27	160	0	146
2015	29	151	1	858
2016	38	202	36	314
2017	31	188	2	577
2018	31	200	1	591
2019	28	160	0	530
2020	38	153	7	458
2021	29	211	0	546
2022	33	142	0	497
2023	51	147	3	618
2024	43	158	0	635
2025	40	147	1	838
2026	23	169	3	—

What is it indicated for?

CAMLOG Implant System Abutments are intended to be used to fabricate crowns and bridges in conjunction with CAMLOG dental implants to support prostheses in the maxillary and/or mandibular arch.

Indications for use as stated in the FDA summary.

https://510kreport.com/device/K073553 · printed Nov 6, 2026

Cite this page

510(k) Report. “K073553: Camlog Implant System Abutments.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K073553

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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