510(k) Report

510(k) · Cleared

Cleared

Progrip™ Self-Gripping Polypropylene Mesh

K232373510(k) TraditionalCleared Jan 18, 2024163-day reviewClass II21 CFR 878.3300

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

Sofradim Production · FTL Mesh, Surgical, Polymeric

Cleared on Jan 18, 2024 as substantially equivalent to K220586 (Sofradim Production, 2022) after a 163-day review. Its family tree reaches back 9 generations to 1999. 2 later devices descend from it.

Decided
Jan 18, 2024
Review
163 days
Class
Class II
Product code
FTL
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K991400 (1999). 35 ancestors in all, the oldest K810428 (1981). 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2018: 1 other ancestor2014: 1 other ancestor2012: 3 other ancestors2011: 4 other ancestors2010: 1 other ancestor2005: 1 other ancestor1999: 1 other ancestor2008: 3 other ancestors2003: 1 other ancestor2002: 2 other ancestors2001: 3 other ancestors1998: 1 other ancestor1993: 2 other ancestors1992: 1 other ancestor1981: 1 other ancestor2025: 1 descendant cleared2026: 1 descendant clearedReference device: K172089 · PROLENE Soft Polypropylene Mesh · ETHICON, Inc. · 2017Reference device: K220540 · ProGrip Self-Gripping Polypropylene Mesh · Covidien · 2022K991400 · Parietene Polypropylene Mesh · Sofradim Production · 1999×2: 2 generations cleared close together, K033376 (2004), K040998 (2004) K081126 · Parietex Composite Mono PM Mesh · Sofradim Production · 2008 · recalledK090858 · Parietex Monofilament Polyester Mesh · Sofradim Production · 2009K131969 · Symbotex (TM) Composite Mesh · Sofradim Production · 2013K142908 · Parietex Monofilament Polyester Mesh (new name: Parietex Lightweight Mesh), Parietex Composite Mono PM Mesh (new name: Parietex Composite Parastomal Mesh), Parietex Composite Ventral Patch, Symbotex Composite Mesh · Sofradim Production · 2014 · recalledK150091 · Versatex Monofilament Mesh · Sofradim Production · 2015 · recalledK220586 · Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh, Parietex Hydrophilic 2D 3D Anatomical Mesh, Versatex Monofilament Mesh · Sofradim Production · 202219801990200020102020
  1. Root · 9 generations backK991400 Parietene Polypropylene MeshSofradim Production · 1999
  2. 5 generations between
  3. 3 generations backK142908 Parietex Monofilament Polyester Mesh (new name: Parietex Lightweight…Sofradim Production · 2014 · Recalled
  4. 2 generations backK150091 Versatex Monofilament MeshSofradim Production · 2015 · Recalled
  5. 1 generation backK220586 Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh…Sofradim Production · 2022
  6. This deviceK232373 Progrip™ Self-Gripping Polypropylene MeshSofradim Production · 2024
  7. Descendant · cites it directly · 1 of its ownK243315 ProGrip™ Self-Gripping Polypropylene MeshSofradim Production · 2025
  8. Descendant · 2 generations on · 0 of its ownK253956 ProGrip™ advanced self-gripping polypropylene mesh (ADG1510…Sofradim Production · 2026
Show all 9 generations
  1. Root · 9 generations backK991400 Parietene Polypropylene MeshSofradim Production · 1999
  2. 8 generations backK033376 Ugytex MeshSofradim Production · 2004
  3. 7 generations backK040998 Modification to Parietex Composite (Pco) MeshSofradim Production · 2004
  4. 6 generations backK081126 Parietex Composite Mono PM MeshSofradim Production · 2008 · Recalled
  5. 5 generations backK090858 Parietex Monofilament Polyester MeshSofradim Production · 2009
  6. 4 generations backK131969 Symbotex (TM) Composite MeshSofradim Production · 2013
  7. 3 generations backK142908 Parietex Monofilament Polyester Mesh (new name: Parietex Lightweight…Sofradim Production · 2014 · Recalled
  8. 2 generations backK150091 Versatex Monofilament MeshSofradim Production · 2015 · Recalled
  9. 1 generation backK220586 Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh…Sofradim Production · 2022
  10. This deviceK232373 Progrip™ Self-Gripping Polypropylene MeshSofradim Production · 2024

Most influential descendants

Showing 2 of 2 · See all
  • K243315ProGrip™ Self-Gripping Polypropylene MeshSofradim Production · 2025 · cites it directly1descendant
  • K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020, ADG4030)Sofradim Production · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K991400Parietene Polypropylene MeshSofradim Production1999—
−8K033376Ugytex MeshSofradim Production2004—
−7K040998Modification to Parietex Composite (Pco) MeshSofradim Production2004—
−6K081126Parietex Composite Mono PM MeshSofradim Production20081
−5K090858Parietex Monofilament Polyester MeshSofradim Production2009—
−4K131969Symbotex (TM) Composite MeshSofradim Production2013—
−3K142908Parietex Monofilament Polyester Mesh (new name: Parietex Lightweight Mesh)…Sofradim Production20141
−2K150091Versatex Monofilament MeshSofradim Production20152
−1K220586Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh, Parietex…Sofradim Production2022—
0 (this device)K232373Progrip™ Self-Gripping Polypropylene MeshSofradim Production2024—
+1K243315ProGrip™ Self-Gripping Polypropylene MeshSofradim Production2025—
+2K253956ProGrip™ advanced self-gripping polypropylene mesh (ADG1510, ADG2015, ADG3020…Sofradim Production2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198110
199210
199320
199810
199910
200130
200220
200310
200510
200830
201010
201140
201230
201410
201810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
202610
FIG. 1 — Lineage of K232373, 1999–2026Source: 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 FTL? 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 FTL device

  1. #1 K220091 Poly-Tape/Infinity-Lock Soft Tissue…score 16.8 · 14 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
*K220586Symbotex Composite Mesh, ProGrip Self-Gripping Polyester Mesh, Parietex Hydrophilic 2D…
Summary page 5
…lassification name: Mesh, Surgical, Polymeric Product code: FTL Regulation number: 21 CFR 878.3300 510(k) Number: K220586 Manufacturer: Sofradim Production (subsidiary of Covidien llc) 116, avenue du Formans…
Sofradim Production2022—
†K172089PROLENE Soft Polypropylene MeshETHICON, Inc.2017—
†K220540ProGrip Self-Gripping Polypropylene MeshCovidien2022—

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K243315ProGrip™ Self-Gripping Polypropylene MeshSofradim Production20251

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 25 years and passes through 1 company; a new generation was cleared every 1.6 years on median.
  • 9 of the 35 ancestors have a recall of any class.
  • Of its descendants, K243315 (Sofradim Production, 2025) has gone furthest, with 1 descendant of its own.

How does its category compare?

All FTL devices

FTL Mesh, Surgical, Polymeric: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · FTL

6in 2025

2007: 202008: 232009: 152010: 182011: 152012: 122013: 82014: 112015: 122016: 32017: 62018: 122019: 42020: 52021: 22022: 62023: 42024: 22025: 62026 (partial year): 2
2007high 23 (2008) · low 2 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FTL

30in 2025

2007: 92 days median2008: 114 days median2009: 97 days median2010: 132 days median2011: 90 days median2012: 213 days median2013: 90 days median2014: 70 days median2015: 121 days median2016: 186 days median2017: 132 days median2018: 105 days median2019: 99 days median2020: 138 days median2022: 195 days median2023: 29 days median2025: 30 days median
2007high 213 (2012) · low 29 (2023)2026

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

Recalls per year · FTL

1in 2020

2007: 22008: 12009: 12010: 122011: 82012: 22013: 12014: 32017: 12018: 12020: 1
2007high 12 (2010) · low 0 (2015)2026

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

Adverse event reports per year · FTL

3,487in 2025

2007: 1,7372008: 1,5692009: 1,9062010: 2,1752011: 3,6082012: 14,7002013: 26,5192014: 2,6832015: 2,5262016: 2,4172017: 3,9472018: 11,8932019: 21,7242020: 18,8192021: 16,2842022: 11,4392023: 8,0252024: 8,5652025: 3,487
2007high 26,519 (2013) · low 1,569 (2008)2025

MAUDE reports naming product code FTL, 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
2007209221,737
20082311411,569
2009159711,906
201018132122,175
2011159083,608
201212213214,700
2013890126,519
2014117032,683
20151212102,526
2016318602,417
2017613213,947
201812105111,893
2019499021,724
20205138118,819
20212—016,284
20226195011,439
202342908,025
20242—08,565
202563003,487
20262—0—

What is it indicated for?

ProGrip™ Self-Gripping Polypropylene Mesh is intended to be used for the reinforcement of abdominal wall soft tissues where weakness exists in procedures involving inguinal and ventral hernia repair by open approach.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K232373: Progrip™ Self-Gripping Polypropylene Mesh.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K232373

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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