Oticon Medical AB
Oticon Medical AB holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2026.
Top product codes for Oticon Medical AB
Recent clearances by Oticon Medical AB
- K261142 — Ponto 5 Mini; Ponto 5 Superpower
- K240614 — Sentio Ti Implant Kit; Sentio 1 Mini; Genie Medical BAHS
- K213733 — Ponto 5 SuperPower
- K211640 — Ponto 5 Mini
- K203807 — Ponto Bone Anchored Hearing System, MONO Surgery Kit
- K190540 — Ponto 4
- K161671 — Ponto 3, Ponto 3 Power and Ponto 3 SuperPower
- K152820 — Ponto Bone Anchored Hearing System
- K152067 — Ponto bone anchored hearing system
- K142678 — Ponto Bone Anchored Hearing system/ Abutment, 14mm. Ponto Bone Anchored Hearing System / Wide implant, 4mm, with abutment, 14 mm
- K141616 — STERILIZATION CASSETTE
- K132775 — PONTO PLUS AND PONTO PLUS POWER
- K121228 — PONTO BONE ANCHORED HEARING SYSTEM
- K112053 — OBC BONE ANCHORED HEARING SYSTEM
- K103594 — PONTO PRO POWER
- K090996 — PONTO PRO
- K082108 — OBC BONE ANCHORED HEARING AID SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.