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AESCULAP

Model ME183R · AESCULAP IMPLANT SYSTEMS, LLC · DI 04046964816673

GEG — Elevator, Surgical, General & Plastic Surgery · Class I · 21 CFR 878.4800

UDILibrary device dossier · generated 2026-09-14 · 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.

11222023-04: 0 reports for this device; peer average 2/device2026-04: 0 reports for this device; peer average 2/device0404
Monthly adverse-event reports for this device versus the product-code average.
MonthThis device (reports)Product-code average (reports per device)
2023-0402
2026-0402
This device (reports/month)Average device in GEG (reports/device/month)

Regulatory clearances

  • None linked in the loaded window.

Manufacturer compliance record — AESCULAP IMPLANT SYSTEMS, LLC

  • NAI 2023-11-09 Aesculap Implant Systems LLC · 0 citations
  • VAI 2021-06-08 Aesculap Implant Systems LLC · 1 citations
  • VAI 2015-03-04 Aesculap Implant Systems LLC · 2 citations
  • NAI 2012-08-27 Aesculap Implant Systems LLC · 0 citations
  • NAI 2010-12-21 Aesculap Implant Systems · 0 citations