510(k) Report

510(k) · Cleared

Cleared

Sharps Containment System

K925816510(k) TraditionalCleared Apr 29, 1994528-day reviewClass II21 CFR 880.5570

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

Post Medical, Inc. · FMI Needle, Hypodermic, Single Lumen

Cleared on Apr 29, 1994 after a 528-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 4 later devices descend from it.

Decided
Apr 29, 1994
Review
528 days
Class
Class II
Product code
FMI
Recalls
None
Predicates
0

4 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared2014: 1 descendant cleared2013: 1 descendant cleared2019: 1 descendant cleared1990200020102020
  1. This deviceK925816 Sharps Containment SystemPost Medical, Inc. · 1994
  2. Descendant · cites it directly · 3 of its ownK982781 Demolizer #47 One-Gallon Point of Generation Sharps ContainerThermal Waste Technology, Inc. · 1998
  3. Descendant · 2 generations on · 1 of its ownK131708 Bwcsh-1 Sharps ContainerBradford Wright Companies, Inc. · 2014
  4. Descendant · 3 generations on · 0 of its ownK182235 OnSite Waste Sharps ContainerBluestone Medical, Inc. · 2019
  5. Descendant · 2 generations on · 0 of its ownK123807 SharpscanMedical Engineering Development Solutions, Inc. · 2013

Most influential descendants

Showing 4 of 4 · See all
  • K982781Demolizer #47 One-Gallon Point of Generation Sharps ContainerThermal Waste Technology, Inc. · 1998 · cites it directly3descendants
  • K131708Bwcsh-1 Sharps ContainerBradford Wright Companies, Inc. · 2014 · 2 generations on1descendant
  • K182235OnSite Waste Sharps ContainerBluestone Medical, Inc. · 2019 · 3 generations on0descendants
  • K123807SharpscanMedical Engineering Development Solutions, Inc. · 2013 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K925816Sharps Containment SystemPost Medical, Inc.1994—
+1K982781Demolizer #47 One-Gallon Point of Generation Sharps ContainerThermal Waste Technology, Inc.1998—
+2K131708Bwcsh-1 Sharps ContainerBradford Wright Companies, Inc.2014—
+3K182235OnSite Waste Sharps ContainerBluestone Medical, Inc.2019—
+2K123807SharpscanMedical Engineering Development Solutions, Inc.2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
201310
201410
201910
FIG. 1 — Lineage of K925816, 1994–2019Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in FMI? 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 FMI device

  1. #1 K252886 Pen Needlescore 14.5 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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? (4)

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

NumberDeviceApplicantDecidedDescendants
K982781Demolizer #47 One-Gallon Point of Generation Sharps ContainerThermal Waste Technology, Inc.19983

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, K982781 (Thermal Waste Technology, Inc., 1998) has gone furthest, with 3 descendants of its own.

How does its category compare?

All FMI devices

FMI Needle, Hypodermic, Single Lumen: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FMI

11in 2025

2007: 152008: 102009: 72010: 152011: 122012: 172013: 112014: 142015: 102016: 202017: 92018: 202019: 122020: 112021: 182022: 232023: 182024: 32025: 112026 (partial year): 12
2007high 23 (2022) · low 3 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FMI

141in 2025

2007: 71 days median2008: 85 days median2009: 177 days median2010: 119 days median2011: 113 days median2012: 107 days median2013: 87 days median2014: 155 days median2015: 89 days median2016: 217 days median2017: 253 days median2018: 176 days median2019: 186 days median2020: 263 days median2021: 143 days median2022: 189 days median2023: 112 days median2024: 90 days median2025: 141 days median2026 (partial year): 119 days median
2007high 263 (2020) · low 71 (2007)2026

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

Recalls per year · FMI

1in 2024

2007: 22008: 42009: 32010: 792011: 52012: 12013: 12014: 32015: 12017: 162019: 52020: 32021: 72023: 22024: 12026 (partial year): 1, 1 Class I
2007high 79 (2010) · low 0 (2016)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FMI

2,424in 2025

2007: 2082008: 1772009: 2632010: 2492011: 2402012: 2152013: 2552014: 2872015: 5672016: 9412017: 1,5472018: 2,3982019: 4,8962020: 4,2452021: 4,5322022: 4,8852023: 4,9862024: 4,0532025: 2,424
2007high 4,986 (2023) · low 177 (2008)2025

MAUDE reports naming product code FMI, 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
200715712208
200810854177
200971773263
20101511979249
2011121135240
2012171071215
201311871255
2014141553287
201510891567
2016202170941
20179253161,547
20182017602,398
20191218654,896
20201126334,245
20211814374,532
20222318904,885
20231811224,986
202439014,053
20251114102,424
2026121191 (1)—
Cite this page

510(k) Report. “K925816: Sharps Containment System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K925816

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