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Anatomical Chin

Model Size: Medium · IMPLANTECH ASSOCIATES, INC. · DI M724ACM1

FWP — Prosthesis, Chin, Internal · Class II · 21 CFR 878.3550

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.

12342019-01: 0 reports for this device; peer average 2/device2019-03: 0 reports for this device; peer average 1.25/device2019-05: 0 reports for this device; peer average 3/device2019-06: 0 reports for this device; peer average 1/device2019-08: 0 reports for this device; peer average 1/device2019-11: 0 reports for this device; peer average 1/device2020-02: 0 reports for this device; peer average 1/device2020-03: 0 reports for this device; peer average 3/device2020-04: 0 reports for this device; peer average 1/device2020-07: 0 reports for this device; peer average 1/device2020-08: 0 reports for this device; peer average 1/device2020-09: 0 reports for this device; peer average 1.33/device2020-10: 0 reports for this device; peer average 1/device2021-03: 0 reports for this device; peer average 1/device2021-05: 0 reports for this device; peer average 4/device2021-06: 0 reports for this device; peer average 2/device2021-08: 0 reports for this device; peer average 1/device2021-09: 0 reports for this device; peer average 2/device2021-10: 0 reports for this device; peer average 1.75/device2021-12: 0 reports for this device; peer average 2/device2022-02: 0 reports for this device; peer average 2/device2022-05: 0 reports for this device; peer average 2/device2022-06: 0 reports for this device; peer average 1.43/device2022-07: 0 reports for this device; peer average 1/device2022-08: 0 reports for this device; peer average 1/device2022-10: 0 reports for this device; peer average 2/device2023-06: 0 reports for this device; peer average 1/device2023-09: 0 reports for this device; peer average 2.5/device2023-10: 0 reports for this device; peer average 1/device2023-11: 0 reports for this device; peer average 1/device2024-05: 0 reports for this device; peer average 1/device2024-06: 0 reports for this device; peer average 1/device2024-09: 0 reports for this device; peer average 1/device2024-10: 0 reports for this device; peer average 1/device2024-11: 0 reports for this device; peer average 2/device2025-01: 0 reports for this device; peer average 1/device2025-04: 0 reports for this device; peer average 1/device2025-05: 0 reports for this device; peer average 1/device2025-06: 0 reports for this device; peer average 1/device2025-08: 0 reports for this device; peer average 1/device2025-09: 0 reports for this device; peer average 2/device2025-10: 0 reports for this device; peer average 1/device2025-12: 0 reports for this device; peer average 1/device2026-03: 0 reports for this device; peer average 1.33/device2026-04: 0 reports for this device; peer average 1/device2026-06: 0 reports for this device; peer average 1/device01030506081102030407080910030506080910120205060708100609101105060910110104050608091012030406
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2019-0102
2019-0301.25
2019-0503
2019-0601
2019-0801
2019-1101
2020-0201
2020-0303
2020-0401
2020-0701
2020-0801
2020-0901.33
2020-1001
2021-0301
2021-0504
2021-0602
2021-0801
2021-0902
2021-1001.75
2021-1202
2022-0202
2022-0502
2022-0601.43
2022-0701
2022-0801
2022-1002
2023-0601
2023-0902.5
2023-1001
2023-1101
2024-0501
2024-0601
2024-0901
2024-1001
2024-1102
2025-0101
2025-0401
2025-0501
2025-0601
2025-0801
2025-0902
2025-1001
2025-1201
2026-0301.33
2026-0401
2026-0601
This device (reports/month)Average device in FWP (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — IMPLANTECH ASSOCIATES, INC.

  • NAI 2015-05-12 Implantech Associates, Inc · 0 citations
  • NAI 2015-05-12 Implantech Associates, Inc · 0 citations
  • NAI 2013-05-03 Implantech Associates, Inc · 0 citations
  • NAI 2013-05-03 Implantech Associates, Inc · 0 citations
  • NAI 2011-08-01 Implantech Associates, Inc · 0 citations
  • NAI 2011-08-01 Implantech Associates, Inc · 0 citations