510(k) Report

510(k) · Cleared

Cleared

NobelDesign Software

K153036510(k) TraditionalCleared Jun 2, 2016227-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

Nobel Biocare AB · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jun 2, 2016 as substantially equivalent to K053602 (Nobel Biocare AB, 2006) after a 227-day review. Its family tree reaches back 4 generations to 2000. 1 later device descends from it.

Decided
Jun 2, 2016
Review
227 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K000018 (2000). 5 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK000018 Branemark NovumNobel Biocare Uas, Inc. · 2000
  2. 3 generations backK030685 Teeth in an Hour - Ark Implant ConceptNobel Biocare AB · 2004 · Recalled
  3. 2 generations backK050393 The Guided Surgery ConceptNobel Biocare AB · 2005
  4. 1 generation backK053602 Procera Software, Model 33145Nobel Biocare AB · 2006
  5. This deviceK153036 NobelDesign SoftwareNobel Biocare AB · 2016
  6. Descendant · cites it directly · 0 of its ownK171466 NobelDesign, DTX Studio DesignNobel Biocare AB · 2017

Most influential descendants

Showing 1 of 1 · See all
  • K171466NobelDesign, DTX Studio DesignNobel Biocare AB · 2017 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K000018Branemark NovumNobel Biocare Uas, Inc.2000—
−3K030685Teeth in an Hour - Ark Implant ConceptNobel Biocare AB20041
−2K050393The Guided Surgery ConceptNobel Biocare AB2005—
−1K053602Procera Software, Model 33145Nobel Biocare AB2006—
0 (this device)K153036NobelDesign SoftwareNobel Biocare AB2016—
+1K171466NobelDesign, DTX Studio DesignNobel Biocare AB2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
FIG. 1 — Lineage of K153036, 2000–2017Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K222288 DESS Dental Smart Solutionsscore 30.6 · 19 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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.

TypeNumberDeviceApplicantDecidedRecalls
*K053602Procera Software, Model 33145
Summary page 4
…Nobel Design Software 1. Predicate Device(s): 510(K) Number Product Name Manufacturer Clearance Date K053602 Procera Software Nobel Biocare Feb 10, 2006 2. Reason for Submission: N…
Nobel Biocare AB2006—

Also cleared against K053602: 2 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K171466NobelDesign, DTX Studio DesignNobel Biocare AB20170

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 16 years and passes through 2 companies; a new generation was cleared every 3.9 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K171466 (Nobel Biocare AB, 2017) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K053602.

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. 2016, this device’s year, is highlighted.

FDA decisions per year · NHA

40in 2025

2007: 382008: 312009: 302010: 192011: 312012: 252013: 222014: 272015: 292016: 382017: 312018: 312019: 282020: 382021: 292022: 332023: 512024: 432025: 402026 (partial year): 23
2007high 51 (2023) · low 19 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NHA

147in 2025

2007: 91 days median2008: 90 days median2009: 95 days median2010: 162 days median2011: 130 days median2012: 171 days median2013: 184 days median2014: 160 days median2015: 151 days median2016: 202 days median2017: 188 days median2018: 200 days median2019: 160 days median2020: 153 days median2021: 211 days median2022: 142 days median2023: 147 days median2024: 158 days median2025: 147 days median2026 (partial year): 169 days median
2007high 211 (2021) · low 90 (2008)2026

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

Recalls per year · NHA

1in 2025

2007: 12008: 22011: 52012: 12013: 12015: 12016: 362017: 22018: 12020: 72023: 32025: 12026 (partial year): 3
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

2007: 12008: 82009: 302010: 612011: 562012: 52013: 1432014: 1462015: 8582016: 3142017: 5772018: 5912019: 5302020: 4582021: 5462022: 4972023: 6182024: 6352025: 838
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
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007389111
2008319028
20093095030
201019162061
201131130556
20122517115
2013221841143
2014271600146
2015291511858
20163820236314
2017311882577
2018312001591
2019281600530
2020381537458
2021292110546
2022331420497
2023511473618
2024431580635
2025401471838
2026231693—

What is it indicated for?

The NobelDesign Software uses patient-specific data from scanners and defines the shapes of dental prosthetic devices such as dental abutments, copings and bridges through the use of a CAD tool. The software also serves as a means of creating, ordering and managing cases.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K153036: NobelDesign Software.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K153036

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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