510(k) Report

510(k) · Cleared

Cleared

Biogel Indicator Underglove with Non-Pyrogenic Statement

K071565510(k) TraditionalCleared Sep 10, 200795-day reviewClass I21 CFR 878.4460

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

Molnlycke Health Care Us, LLC · KGO Surgeon'S Gloves

Cleared on Sep 10, 2007 as substantially equivalent to K980942 (London International Group, Inc., 1998) and 1 other predicate after a 95-day review. Its family tree reaches back 2 generations to 2004. 1 later device descends from it.

Decided
Sep 10, 2007
Review
95 days
Class
Class I
Product code
KGO
Recalls
None
Predicates
2

Its longest line of descent runs back 2 generations to K033564 (2004). 3 ancestors in all, the oldest K980942 (1998). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1998: 1 other ancestor2010: 1 descendant clearedK033564 · Powder Free Latex Surgeons Gloves Polymer Coated Sterile with Optional Labeling Claim of E.P. Less Than 50 UG/DM2 · Kanam Latex Industries Pvt., Ltd. · 2004K060030 · The Double Glove · Biobarrier, Inc. · 20061995200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor 1 generation forward: 1 descendant K060030 · The Double Glove · Biobarrier, Inc. · 2006K033564 · Powder Free Latex Surgeons Gloves Polymer Coated Sterile with Optional Labeling Claim of E.P. Less Than 50 UG/DM2 · Kanam Latex Industries Pvt., Ltd. · 20040
  1. Root · 2 generations backK033564 Powder Free Latex Surgeons Gloves Polymer Coated Sterile with…Kanam Latex Industries Pvt., Ltd. · 2004
  2. 1 generation backK060030 The Double GloveBiobarrier, Inc. · 2006
  3. This deviceK071565 Biogel Indicator Underglove with Non-Pyrogenic StatementMolnlycke Health Care Us, LLC · 2007
  4. Descendant · cites it directly · 0 of its ownK101163 Biogel Orthopro Indicator UndergloveMolnlycke Health Care USA · 2010

Most influential descendants

Showing 1 of 1 · See all
  • K101163Biogel Orthopro Indicator UndergloveMolnlycke Health Care USA · 2010 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K033564Powder Free Latex Surgeons Gloves Polymer Coated Sterile with Optional…Kanam Latex Industries Pvt., Ltd.2004—
−1K060030The Double GloveBiobarrier, Inc.2006—
0 (this device)K071565Biogel Indicator Underglove with Non-Pyrogenic StatementMolnlycke Health Care Us, LLC2007—
+1K101163Biogel Orthopro Indicator UndergloveMolnlycke Health Care USA2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
FIG. 1 — Lineage of K071565, 2004–2010Source: 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 KGO? 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 KGO device

  1. #1 K192328 JR.MEDIK Latex Surgeon’s Gloves Powder Freescore 15.2 · 5 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
*K980942Regent Biogel Indicator Inner Surgical Glove
Summary page 1
…lassification: Surgical Glove (CFR 878.4461) Class I 4. Predicate Device: K980942 - Biogel® lndicatorTM Underglove K060030 - Eclipse, Non-pyrogenic, Latex, Powder-…
London International Group, Inc.1998—
*K060030The Double Glove
Summary page 1
…Class I 4. Predicate Device: K980942 - Biogel® lndicatorTM Underglove K060030 - Eclipse, Non-pyrogenic, Latex, Powder-free, Glove 5. Device Description: The Biogel® IndicatorTM Under…
Biobarrier, Inc.2006—

Also cleared against K980942: 2 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K101163Biogel Orthopro Indicator UndergloveMolnlycke Health Care USA20100

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 3 years and passes through 3 companies; a new generation was cleared every 2.3 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K101163 (Molnlycke Health Care USA, 2010) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K980942.

How does its category compare?

All KGO devices

KGO Surgeon'S Gloves: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · KGO

1in 2025

2007: 102008: 22009: 32010: 62011: 112012: 72013: 62014: 72015: 122016: 92017: 122018: 72019: 112020: 152021: 142022: 62023: 142024: 22025: 12026 (partial year): 2
2007high 15 (2020) · low 1 (2025)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KGO

185in 2023

2007: 113 days median2009: 48 days median2010: 87 days median2011: 90 days median2012: 133 days median2013: 184 days median2014: 257 days median2015: 225 days median2016: 218 days median2017: 111 days median2018: 194 days median2019: 204 days median2020: 117 days median2021: 199 days median2022: 127 days median2023: 185 days median
2007high 257 (2014) · low 48 (2009)2026

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

Recalls per year · KGO

2in 2023

2009: 152010: 12016: 22017: 12018: 82022: 22023: 2
2007high 15 (2009) · low 0 (2007)2026

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

Adverse event reports per year · KGO

21in 2025

2007: 132008: 82009: 142010: 162011: 142012: 142013: 412014: 282015: 112016: 152017: 202018: 152019: 512020: 152021: 142022: 102023: 282024: 182025: 21
2007high 51 (2019) · low 8 (2008)2025

MAUDE reports naming product code KGO, 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
200710113013
20082—08
20093481514
2010687116
20111190014
20127133014
20136184041
20147257028
201512225011
20169218215
201712111120
20187194815
201911204051
202015117015
202114199014
20226127210
202314185228
20242—018
20251—021
20262—0—

What is it indicated for?

The Biogel® IndicatorTM Underglove is a disposable device made of natural rubber latex that is intended to be worn on the hands, usually in a surgical setting, to provide a barrier against potentially infectious material and other contaminants.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071565: Biogel Indicator Underglove with Non-Pyrogenic Statement.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071565

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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