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Game Ready Med4 Elite Therapy Hose Assembly - Patient 2

Model 503648 · Avanos Medical, Inc. · DI 00812120004048

ILOPack, Hot Or Cold, Water Circulating · Class II · 21 CFR 890.5720

IRPMassager, Powered Inflatable Tube · Class II · 21 CFR 890.5650

UDILibrary device dossier · generated 2026-09-07 · 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.

23562019-01: 0 reports for this device; peer average 2/device2019-04: 0 reports for this device; peer average 1.67/device2019-05: 0 reports for this device; peer average 1.5/device2019-06: 0 reports for this device; peer average 3/device2019-07: 0 reports for this device; peer average 2/device2019-08: 0 reports for this device; peer average 1.4/device2019-10: 0 reports for this device; peer average 1.33/device2020-02: 0 reports for this device; peer average 2/device2020-07: 0 reports for this device; peer average 1/device2020-10: 0 reports for this device; peer average 1.5/device2020-11: 0 reports for this device; peer average 2/device2021-01: 0 reports for this device; peer average 1/device2021-02: 0 reports for this device; peer average 3/device2021-04: 0 reports for this device; peer average 1.25/device2021-05: 0 reports for this device; peer average 2/device2021-06: 0 reports for this device; peer average 2/device2021-07: 0 reports for this device; peer average 1/device2021-08: 0 reports for this device; peer average 2/device2021-11: 0 reports for this device; peer average 1/device2022-03: 0 reports for this device; peer average 4/device2022-04: 0 reports for this device; peer average 1/device2022-05: 0 reports for this device; peer average 1/device2022-08: 0 reports for this device; peer average 4/device2022-09: 0 reports for this device; peer average 1/device2022-10: 0 reports for this device; peer average 2/device2022-12: 0 reports for this device; peer average 1/device2023-01: 0 reports for this device; peer average 2/device2023-02: 0 reports for this device; peer average 1.5/device2023-03: 0 reports for this device; peer average 1/device2023-04: 0 reports for this device; peer average 1/device2023-05: 0 reports for this device; peer average 2/device2023-06: 0 reports for this device; peer average 1/device2023-11: 0 reports for this device; peer average 1/device2024-03: 0 reports for this device; peer average 2/device2024-04: 0 reports for this device; peer average 2/device2024-05: 0 reports for this device; peer average 2/device2024-10: 0 reports for this device; peer average 1/device2024-11: 0 reports for this device; peer average 3.33/device2025-01: 0 reports for this device; peer average 6/device2025-03: 0 reports for this device; peer average 1/device2025-04: 0 reports for this device; peer average 1/device2025-07: 0 reports for this device; peer average 1.5/device2025-09: 0 reports for this device; peer average 1/device2025-10: 0 reports for this device; peer average 1/device2026-01: 0 reports for this device; peer average 1/device010405060708100207101101020405060708110304050809101201020304050611030405101101030407091001
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0102
2019-0401.67
2019-0501.5
2019-0603
2019-0702
2019-0801.4
2019-1001.33
2020-0202
2020-0701
2020-1001.5
2020-1102
2021-0101
2021-0203
2021-0401.25
2021-0502
2021-0602
2021-0701
2021-0802
2021-1101
2022-0304
2022-0401
2022-0501
2022-0804
2022-0901
2022-1002
2022-1201
2023-0102
2023-0201.5
2023-0301
2023-0401
2023-0502
2023-0601
2023-1101
2024-0302
2024-0402
2024-0502
2024-1001
2024-1103.33
2025-0106
2025-0301
2025-0401
2025-0701.5
2025-0901
2025-1001
2026-0101
This device (reports/month)Average device in ILO, IRP (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Predicate lineage

K171685 — cites (transitively): K061866 (d1), K072620 (d1) — cited as predicate by K181149, K183702, K190854, K193079, K193550, K222136, K242754, K252386, K252396

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

Manufacturer compliance record — Avanos Medical, Inc.

  • Warning Letter 2013-04-10 Avanos Medical, Inc.
  • Warning Letter 2013-04-10 Avanos Medical, Inc.
  • Warning Letter 2008-12-22 Avanos Medical, Inc.
  • Warning Letter 2008-12-22 Avanos Medical, Inc.
  • VAI 2023-12-15 Avanos Medical, Inc. · 3 citations
  • VAI 2023-12-15 Avanos Medical, Inc. · 3 citations
  • VAI 2018-10-02 Avanos Medical, Inc. · 1 citations
  • VAI 2018-10-02 Avanos Medical, Inc. · 1 citations
  • VAI 2016-07-29 Avanos Medical, Inc. · 1 citations
  • VAI 2016-07-29 Avanos Medical, Inc. · 1 citations
  • NAI 2014-11-05 Avanos Medical, Inc. · 0 citations
  • NAI 2014-11-05 Avanos Medical, Inc. · 0 citations
  • VAI 2014-03-07 Avanos Medical, Inc. · 4 citations
  • VAI 2014-03-07 Avanos Medical, Inc. · 4 citations
  • NAI 2013-12-10 Avanos Medical, Inc. · 0 citations
  • NAI 2013-12-10 Avanos Medical, Inc. · 0 citations
  • OAI 2013-01-04 Avanos Medical, Inc. · 6 citations
  • OAI 2013-01-04 Avanos Medical, Inc. · 6 citations
  • OAI 2012-10-31 Avanos Medical, Inc. · 10 citations
  • OAI 2012-10-31 Avanos Medical, Inc. · 10 citations
  • VAI 2011-07-08 Avanos Medical, Inc. · 8 citations
  • VAI 2011-07-08 Avanos Medical, Inc. · 8 citations
  • OAI 2010-11-19 Avanos Medical, Inc. · 4 citations
  • OAI 2010-11-19 Avanos Medical, Inc. · 4 citations