510(k) Report

510(k) · Cleared

Cleared

Panthera Dental Milled Bars

K183580510(k) AbbreviatedCleared Jun 20, 2019181-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

Panthera Dental, Inc. · NHA Abutment, Implant, Dental, Endosseous

Cleared on Jun 20, 2019 as substantially equivalent to K173466 (Panthera Dental, Inc., 2018) after a 181-day review. Its family tree reaches back 8 generations to 1995.

Decided
Jun 20, 2019
Review
181 days
Class
Class II
Product code
NHA
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K944964 (1995). 23 ancestors in all, the oldest K910611 (1991). No later device cites it as a predicate yet.

  1. Root · 8 generations backK944964 Branemark System Miruscone Abutment SystemNobelpharma USA, Inc. · 1995
  2. 7 generations backK961728 Miruscone Abutment SystemNobelpharma USA, Inc. · 1996
  3. 6 generations backK962403 Noblepharma Wide AccessoriesNobelpharma USA, Inc. · 1996
  4. 5 generations backK971706 Tiadapt Abutment SystemNobel Biocare Uas, Inc. · 1997
  5. 4 generations backK974150 Procera Preparable Abutment SystemNobel Biocare Uas, Inc. · 1998 · Recalled
  6. 3 generations backK034035 3I Patient-Specific Overdenture BarImplant Innovations, Inc. · 2004
  7. 2 generations backK080864 Cam Structsure Precision Milled BarsBiomet 3i, Inc. · 2008
  8. 1 generation backK173466 Panthera Dental Milled BarsPanthera Dental, Inc. · 2018
  9. This deviceK183580 Panthera Dental Milled BarsPanthera Dental, Inc. · 2019
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K944964Branemark System Miruscone Abutment SystemNobelpharma USA, Inc.1995—
−7K961728Miruscone Abutment SystemNobelpharma USA, Inc.1996—
−6K962403Noblepharma Wide AccessoriesNobelpharma USA, Inc.1996—
−5K971706Tiadapt Abutment SystemNobel Biocare Uas, Inc.1997—
−4K974150Procera Preparable Abutment SystemNobel Biocare Uas, Inc.19982
−3K0340353I Patient-Specific Overdenture BarImplant Innovations, Inc.2004—
−2K080864Cam Structsure Precision Milled BarsBiomet 3i, Inc.2008—
−1K173466Panthera Dental Milled BarsPanthera Dental, Inc.2018—
0 (this device)K183580Panthera Dental Milled BarsPanthera Dental, Inc.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199380
199420
199530
199610
FIG. 1 — Lineage of K183580, 1995–2019Source: 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 30.7 · 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
*K173466Panthera Dental Milled Bars
Summary page 4
…mon Name: Overdenture Bar Classification: 21 CFR 872.3630 (Class II) Product: NHA Primary Predicate: K173466 Panthera Dental Milled Bars Reference Devices: K140737 Straumann CARES Screw-Retained Bars/Bridges…
Panthera Dental, Inc.2018—
†K140737Straumann Cares Screw Retained Bars/BridgeStraumann USA, LLC2014—
†K171784Straumann Dental Implant SystemStraumann USA, LLC2018—
†K140878Straumann Bone Level Tapered ImplantStraumann USA, LLC20142
†K111357Straumann Narrow Neck Crossfit (NNC) 03.3MM Dental Implant SystemStraumann USA2011—

Also cleared against K173466: 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 24 years and passes through 5 companies; a new generation was cleared every 1.4 years on median.
  • 1 of the 23 ancestors has a recall of any class.
  • 1 other device also cites its predicate K173466.

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. 2019, 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 Panthera Dental Milled Bar is indicated for use as an accessory to an endosseous dental implant to support a prosthetic device in a partially or edentulous patient for purpose of restoring chewing function. It is intended for use to support multiple tooth prostheses in the mandible or maxilla. The prostheses can be screw retained. The Panthera Dental Milled Bars are indicated for compatibility with: • Standard/Standard Plus RN – Ø 4.1/4.8 (platform Ø…

Read the full statement (126 words)

The Panthera Dental Milled Bar is indicated for use as an accessory to an endosseous dental implant to support a prosthetic device in a partially or edentulous patient for purpose of restoring chewing function. It is intended for use to support multiple tooth prostheses in the mandible or maxilla. The prostheses can be screw retained.

The Panthera Dental Milled Bars are indicated for compatibility with:

• Standard/Standard Plus RN – Ø 4.1/4.8 (platform Ø 4.8)

• Standard/ Standard Plus/Tapered Effect WN - Ø 4.8 (platform Ø 6.5)

• Tapered Effect RN - Ø 4.1 (platform Ø 4.8)

• Bone Level/ Bone Level Tapered NC - Ø 3.3 (platform Ø 3.3)

• Bone Level/ Bone Level Tapered RC - Ø 4.1, 4.8 (platforms Ø 4.1 and 4.8)

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. “K183580: Panthera Dental Milled Bars.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K183580

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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