510(k) Report

510(k) · Cleared

Cleared

Blue Sky Bio Computerized Orthodontic Bracket System

K182338510(k) TraditionalCleared Nov 9, 201873-day reviewClass II21 CFR 872.5470

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

Blue Sky Bio · DYW Bracket, Plastic, Orthodontic

Cleared on Nov 9, 2018 after a 73-day review. The summary cites one number, which could not be confirmed as its predicate (see the table below).

Decided
Nov 9, 2018
Review
73 days
Class
Class II
Product code
DYW
Recalls
None
Predicates
1

The summary cites one number, which could not be confirmed as its predicate (see the table below).

FIG. 1 — Lineage of K182338Source: FDA 510(k) database · 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 DYW? 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 DYW device

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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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
Kept off the family treeK151702FDA’s K151702 is Reusable Full Silicone Cover
Our reading of the summary gave K151702, FDA’s number for Reusable Full Silicone Cover (Laerdal Medical AS). Its FDA name has none of the distinctive words the summary uses for the device it names, “Exceed Computerized Precision Bracket Placement Solution”. Kept off the family tree.
Summary page 7
…Class II Page 1 of 5 24 Predicate 510k: Exceed Computerized Precision Bracket Placement Solution K151702 Indications for Use: Blue Sky Bio Computerized Bracket System is a software system intended for use as an aid in orthodontic trea…
Laerdal Medical AS2015—

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.

How does its category compare?

All DYW devices

DYW Bracket, Plastic, Orthodontic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · DYW

2in 2025

2007: 22008: 12009: 22010: 12011: 12012: 12013: 22014: 12016: 32018: 22020: 12025: 2
2007high 3 (2016) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DYW

372in 2016

2016: 372 days median
2007high 372 (2016)2026

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

Recalls per year · DYW

2in 2011

2011: 2
2007high 2 (2011) · low 0 (2007)2026

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

Adverse event reports per year · DYW

1in 2017

2007: 22014: 42015: 42017: 1
2007high 4 (2014) · low 0 (2008)2025

MAUDE reports naming product code DYW, 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
20072—02
20081—00
20092—00
20101—00
20111—20
20121—00
20132—00
20141—04
20150—04
2016337200
20170—01
20182—00
20190—00
20201—00
20210—00
20220—00
20230—00
20240—00
20252—00
20260—0—

What is it indicated for?

Blue Sky Bio Computerized Orthodontic Bracket System is a software system intended for use as an aid in orthodontic treatment planning to correct malocclusions in orthodontic patients. For use by dental professionals trained in orthodontic treatment, including radiographic analyses and treatment planning. Blue Sky Bio Computerized Orthodontic Bracket System is intended for use with commercially available brackets currently used in standard orthodontic treatment. The end product is an indirect bonding tray for use by the dental professional to place multiple brackets at the same time.

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. “K182338: Blue Sky Bio Computerized Orthodontic Bracket System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K182338

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026