510(k) Report

510(k) · Cleared

Cleared

Insulin Pen Needle

K120690510(k) TraditionalCleared Jun 22, 2012107-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

Tiger Medical Products, Ltd. · FMI Needle, Hypodermic, Single Lumen

Cleared on Jun 22, 2012 as substantially equivalent to K051899 (Becton, Dickinson & CO, 2005) and 1 other predicate after a 107-day review. Its family tree reaches back 4 generations to 1997. 20 later devices descend from it.

Decided
Jun 22, 2012
Review
107 days
Class
Class II
Product code
FMI
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K973899 (1997). 6 ancestors in all. 20 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2010: 1 other ancestor2014: 2 descendants cleared2016: 2 descendants cleared2017: 2 descendants cleared2018: 1 descendant cleared2021: 4 descendants cleared2019: 1 descendant cleared2024: 1 descendant cleared2020: 2 descendants cleared2022: 2 descendants cleared2026: 1 descendant cleared2023: 2 descendants clearedK973899 · Unifine Pentips · Owen Mumford USA, Inc. · 1997K033575 · One.Click Needle · B.Braun Medical, Inc. · 2004K080904 · Feel-Fine Insulin Pen Needle · Feel Tech · 2008 · recalledK112332 · Fine Ject Insulin Pen Needle · Twobiens Co., Ltd. · 20121995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor 1 generation forward: 2 descendants2 generations forward: 4 descendants3 generations forward: 9 descendants4 generations forward: 5 descendants K112332 · Fine Ject Insulin Pen Needle · Twobiens Co., Ltd. · 2012K080904 · Feel-Fine Insulin Pen Needle · Feel Tech · 2008 · recalledK033575 · One.Click Needle · B.Braun Medical, Inc. · 2004K973899 · Unifine Pentips · Owen Mumford USA, Inc. · 19970
  1. Root · 4 generations backK973899 Unifine PentipsOwen Mumford USA, Inc. · 1997
  2. 3 generations backK033575 One.Click NeedleB.Braun Medical, Inc. · 2004
  3. 2 generations backK080904 Feel-Fine Insulin Pen NeedleFeel Tech · 2008 · Recalled
  4. 1 generation backK112332 Fine Ject Insulin Pen NeedleTwobiens Co., Ltd. · 2012
  5. This deviceK120690 Insulin Pen NeedleTiger Medical Products, Ltd. · 2012
  6. Descendant · cites it directly · 18 of its ownK133059 Insulin Pen NeedleWenzhou Beipu Science & Technology Co., Ltd. · 2014
  7. Descendant · 2 generations on · 9 of its ownK161950 Common Type Insulin Pen Needle, Safety Type Insulin Pen NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2017
  8. Descendant · 2 generations on · 3 of its ownK181069 Disposable Insulin Pen NeedleZhejiang Kindly Medical Devices Co., Ltd. · 2018
  9. Descendant · 2 generations on · 2 of its ownK152824 Medt Pen NeedleShandong Caremed Medical Products Co., Ltd. · 2016
  10. Descendant · 3 generations on · 1 of its ownK202319 Insulin Pen Needle (Ordinary Type), Insulin Pen Needle (Safety Type)Tianjin Huahong Technology Co., Ltd. · 2021

Showing 5 of 20 descendants. See all descendants

Descendants cleared per year

2014: 22016: 22017: 22018: 12019: 12020: 22021: 42022: 22023: 22024: 12026: 1
2014high 4 (2021) · low 0 (2015)2026

Most influential descendants

Showing 5 of 20 · See all
  • K133059Insulin Pen NeedleWenzhou Beipu Science & Technology Co., Ltd. · 2014 · cites it directly18descendants
  • K161950Common Type Insulin Pen Needle, Safety Type Insulin Pen NeedlePromisemed Hangzhou Meditech Co., Ltd. · 2017 · 2 generations on9descendants
  • K181069Disposable Insulin Pen NeedleZhejiang Kindly Medical Devices Co., Ltd. · 2018 · 2 generations on3descendants
  • K152824Medt Pen NeedleShandong Caremed Medical Products Co., Ltd. · 2016 · 2 generations on2descendants
  • K202319Insulin Pen Needle (Ordinary Type), Insulin Pen Needle (Safety Type)Tianjin Huahong Technology Co., Ltd. · 2021 · 3 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K973899Unifine PentipsOwen Mumford USA, Inc.1997—
−3K033575One.Click NeedleB.Braun Medical, Inc.2004—
−2K080904Feel-Fine Insulin Pen NeedleFeel Tech20087
−1K112332Fine Ject Insulin Pen NeedleTwobiens Co., Ltd.2012—
0 (this device)K120690Insulin Pen NeedleTiger Medical Products, Ltd.2012—
+1K133059Insulin Pen NeedleWenzhou Beipu Science & Technology Co., Ltd.2014—
+2K161950Common Type Insulin Pen Needle, Safety Type Insulin Pen NeedlePromisemed Hangzhou Meditech Co., Ltd.2017—
+2K181069Disposable Insulin Pen NeedleZhejiang Kindly Medical Devices Co., Ltd.2018—
+2K152824Medt Pen NeedleShandong Caremed Medical Products Co., Ltd.2016—
+3K202319Insulin Pen Needle (Ordinary Type), Insulin Pen Needle (Safety Type)Tianjin Huahong Technology Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200510
201010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201420
201620
201720
201810
201910
202020
202140
202220
202320
202410
202610
FIG. 1 — Lineage of K120690, 1997–2026Source: 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 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
Get a 510(k) Report

What was it cleared against? (2)

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
*K051899BD Pen Needle
Summary page 1
…lin pen needle b. Regulation Number: 880.5570 c. Product code: EMI d. Class: 11 e. Review Panel: General Hospital 5. Predicate Device Identification: K05 1899 Trade Name: BD Pen Needles K112332 Trade Name: Fine Ject Insulin Pen Needle 6. Device Description: Insulin pen needl…
Becton, Dickinson & CO2005—
*K112332Fine Ject Insulin Pen Needle
Summary page 1
….5570 c. Product code: EMI d. Class: 11 e. Review Panel: General Hospital 5. Predicate Device Identification: K05 1899 Trade Name: BD Pen Needles K112332 Trade Name: Fine Ject Insulin Pen Needle 6. Device Description: Insulin pen needle is a single-use device, which consists of…
Twobiens Co., Ltd.2012—

Also cleared against K051899: 13 other devices →

What descends from it? (20)

See all 20

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

NumberDeviceApplicantDecidedDescendants
K133059Insulin Pen NeedleWenzhou Beipu Science & Technology Co., Ltd.201418
K133058Insulin Pen NeedleWenzhou Wuzhou Import & Export Co., Ltd.20140

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 15 years and passes through 5 companies; a new generation was cleared every 4.3 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K133059 (Wenzhou Beipu Science & Technology Co., Ltd., 2014) has gone furthest, with 18 descendants of its own.
  • 13 other devices also cite its predicate K051899.

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. 2012, this device’s year, is highlighted.

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)—

What is it indicated for?

Insulin pen needle is intended for use with pen injector for subcutaneous injection of

insulin.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K120690: Insulin Pen Needle.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K120690

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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