Skip to content
Print-ready dossier — use your browser's print dialog to save as PDF.

TRIPLE PLAY

Model TP3434 · Compression Solutions, LLC · DI 04042809585940

JOWSleeve, Limb, Compressible · Class II · 21 CFR 870.5800

UDILibrary device dossier · generated 2026-09-11 · sources: FDA GUDID, openFDA (recalls, MAUDE, 510(k)/PMA), FDA Data Dashboard (inspections, compliance actions), 510(k) summary documents.

Recall history (0)

No recalls linked in the loaded window.

Adverse-event reports — MAUDE (0)

Caveat (required reading): MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line is a reporting baseline (average device in the same product code), not a risk measure.

51014192019-01: 0 reports for this device; peer average 1/device2019-05: 0 reports for this device; peer average 2/device2019-06: 0 reports for this device; peer average 2.33/device2019-07: 0 reports for this device; peer average 1/device2019-08: 0 reports for this device; peer average 11/device2019-09: 0 reports for this device; peer average 1.33/device2019-10: 0 reports for this device; peer average 2/device2019-11: 0 reports for this device; peer average 1/device2019-12: 0 reports for this device; peer average 19/device2020-02: 0 reports for this device; peer average 4.25/device2020-03: 0 reports for this device; peer average 1.5/device2020-07: 0 reports for this device; peer average 2/device2020-08: 0 reports for this device; peer average 1/device2020-09: 0 reports for this device; peer average 1.5/device2020-12: 0 reports for this device; peer average 1/device2021-01: 0 reports for this device; peer average 1.33/device2021-02: 0 reports for this device; peer average 2/device2021-03: 0 reports for this device; peer average 1/device2021-04: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 1/device2021-06: 0 reports for this device; peer average 4/device2021-07: 0 reports for this device; peer average 1/device2021-09: 0 reports for this device; peer average 1/device2021-10: 0 reports for this device; peer average 1/device2021-11: 0 reports for this device; peer average 3/device2022-03: 0 reports for this device; peer average 1.5/device2022-05: 0 reports for this device; peer average 2/device2022-06: 0 reports for this device; peer average 1.5/device2022-08: 0 reports for this device; peer average 4/device2023-02: 0 reports for this device; peer average 3/device2023-03: 0 reports for this device; peer average 6.5/device2023-07: 0 reports for this device; peer average 2/device2023-08: 0 reports for this device; peer average 2/device2023-09: 0 reports for this device; peer average 1/device2023-10: 0 reports for this device; peer average 4/device2023-11: 0 reports for this device; peer average 1.5/device2024-02: 0 reports for this device; peer average 1/device2024-04: 0 reports for this device; peer average 1.5/device2024-05: 0 reports for this device; peer average 1.33/device2024-06: 0 reports for this device; peer average 1.5/device2024-07: 0 reports for this device; peer average 2/device2024-11: 0 reports for this device; peer average 2/device2024-12: 0 reports for this device; peer average 1/device2025-01: 0 reports for this device; peer average 2/device2025-02: 0 reports for this device; peer average 1.67/device2025-07: 0 reports for this device; peer average 2/device2025-08: 0 reports for this device; peer average 3/device2025-10: 0 reports for this device; peer average 1/device2026-03: 0 reports for this device; peer average 1.75/device2026-04: 0 reports for this device; peer average 6.67/device2026-05: 0 reports for this device; peer average 4.25/device2026-06: 0 reports for this device; peer average 2.83/device01050607080910111202030708091201020304050607091011030506080203070809101102040506071112010207081003040506
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0101
2019-0502
2019-0602.33
2019-0701
2019-08011
2019-0901.33
2019-1002
2019-1101
2019-12019
2020-0204.25
2020-0301.5
2020-0702
2020-0801
2020-0901.5
2020-1201
2021-0101.33
2021-0202
2021-0301
2021-0401
2021-0501
2021-0604
2021-0701
2021-0901
2021-1001
2021-1103
2022-0301.5
2022-0502
2022-0601.5
2022-0804
2023-0203
2023-0306.5
2023-0702
2023-0802
2023-0901
2023-1004
2023-1101.5
2024-0201
2024-0401.5
2024-0501.33
2024-0601.5
2024-0702
2024-1102
2024-1201
2025-0102
2025-0201.67
2025-0702
2025-0803
2025-1001
2026-0301.75
2026-0406.67
2026-0504.25
2026-0602.83
This device (reports/month)Average device in JOW (reports/device/month)

Regulatory clearances

  • K103187 SESE 2011-01-26 (k number procode)

Predicate lineage

K103187 — cites (transitively): K022340 (d1), K023573 (d1), K061125 (d1), K061866 (d1) — cited as predicate by K130174, K133274

Lineage extracted from public 510(k) summary text (heuristic).

Manufacturer compliance record — Compression Solutions, LLC

  • VAI 2013-06-13 Compression Solutions LLC · 5 citations
  • VAI 2013-06-13 Compression Solutions LLC · 5 citations