510(k) Report

510(k) · Cleared

Cleared

Oxboro-Medical Pin Covers

K952783510(k) TraditionalCleared Sep 15, 199588-day reviewClass II21 CFR 888.3030

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

Oxboro Medical Intl., Inc. · LRN Wire, Surgical

Cleared on Sep 15, 1995 after an 88-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Sep 15, 1995
Review
88 days
Class
Class II
Product code
LRN
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K952783Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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  • Recall history across each candidate’s familyin the report
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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 LRN devices

LRN Wire, Surgical: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LRN

FDA has decided no LRN device since 2007.

Median 510(k) review, days · LRN

Too few LRN 510(k)s in any year since 2007 to give a median.

Recalls per year · LRN

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · LRN

81in 2025

2007: 32008: 202009: 312010: 132011: 62012: 252013: 1082014: 572015: 242016: 382017: 332018: 582019: 842020: 682021: 1182022: 1062023: 1402024: 872025: 81
2007high 140 (2023) · low 3 (2007)2025

MAUDE reports naming product code LRN, 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
20070—03
20080—020
20090—031
20100—013
20110—06
20120—025
20130—0108
20140—057
20150—024
20160—038
20170—033
20180—058
20190—184
20200—068
20210—0118
20220—0106
20230—0140
20240—087
20250—081
20260—0—
Cite this page

510(k) Report. “K952783: Oxboro-Medical Pin Covers.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K952783

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Record history
  • FDA decision record loaded May 2, 2026
  • Page last updated Nov 3, 2026