510(k) Report

510(k) · Cleared

Cleared

DTX-200 Bone Densitometer

K964562510(k) TraditionalCleared Aug 22, 1997282-day reviewClass II21 CFR 892.1170

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

Osteometer Meditech A/S · KGI Densitometer, Bone

Cleared on Aug 22, 1997 after a 282-day review. The FDA summary names its predicate without a number. 2 later devices descend from it.

Decided
Aug 22, 1997
Review
282 days
Class
Class II
Product code
KGI
Recalls
None
Predicates
0

2 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2002: 1 descendant cleared1995200020052010201520202025
  1. This deviceK964562 DTX-200 Bone DensitometerOsteometer Meditech A/S · 1997
  2. Descendant · cites it directly · 0 of its ownK033550 DXL CalscanDemetech AB · 2004
  3. Descendant · cites it directly · 0 of its ownK021331 Dexacare G4Osteometer Meditech, Inc. · 2002

Most influential descendants

Showing 2 of 2 · See all
  • K033550DXL CalscanDemetech AB · 2004 · cites it directly0descendants
  • K021331Dexacare G4Osteometer Meditech, Inc. · 2002 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K964562DTX-200 Bone DensitometerOsteometer Meditech A/S1997—
+1K033550DXL CalscanDemetech AB2004—
+1K021331Dexacare G4Osteometer Meditech, Inc.2002—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200210
200410
FIG. 1 — Lineage of K964562, 1997–2004Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 KGI? 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 KGI device

  1. #1 K252718 Lunar Astrascore 13.3 · 8 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
*—Osteometer MediTech A/S model DTX-200 bone densitometer
Named without a submission number
—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K033550DXL CalscanDemetech AB20040
K021331Dexacare G4Osteometer Meditech, Inc.20020

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, K033550 (Demetech AB, 2004) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KGI devices

KGI Densitometer, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KGI

3in 2025

2007: 22008: 52009: 12011: 22012: 52013: 12014: 22016: 22018: 12019: 12022: 22023: 12025: 32026 (partial year): 2
2007high 5 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGI

156in 2025

2008: 173 days median2012: 142 days median2025: 156 days median
2007high 173 (2008) · low 142 (2012)2026

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

Recalls per year · KGI

1in 2016

2008: 62009: 92011: 12016: 1
2007high 9 (2009) · low 0 (2007)2026

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

Adverse event reports per year · KGI

8in 2025

2008: 22009: 32011: 52012: 12013: 12014: 22016: 12017: 162018: 62020: 22021: 12022: 12023: 22024: 22025: 8
2007high 16 (2017) · low 0 (2007)2025

MAUDE reports naming product code KGI, 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—00
2008517362
20091—93
20100—00
20112—15
2012514201
20131—01
20142—02
20150—00
20162—11
20170—016
20181—06
20191—00
20200—02
20210—01
20222—01
20231—02
20240—02
2025315608
20262—0—

What is it indicated for?

Estimate bone mineral

content (BMC in grams) and bone mineral density (BMD in

grams/cm®) in the distal section of the forearm.

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. “K964562: DTX-200 Bone Densitometer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K964562

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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