ApprovalTrail

Medical device licence · 2467 · Class 2

IN-THE-EAR HEARING AID

No longer licensed: cancelled

Licence status Cancelled; first licensed April 21, 1999; ended June 19, 2024. It is in Health Canada’s archive of licences no longer in force.
Licence number
2467
Licence holder
Oticon ASmorum, Denmark
Risk class
Class II (low to moderate risk)
Licence type
Device Family
First licensed
April 21, 1999
Ended
June 19, 2024
Devices covered
55

Devices on this licence

By name, as listed. The official record lists model numbers and identifiers.

  • ACTO PRO-ITE
  • ACTO-ITE
  • ADAPTO - ITE
  • AGIL - ITE
  • AGIL PRO-ITE
  • ALTA - ITE
  • ALTA 2 ITE
  • ALTA 2 PRO ITE
  • ALTA PRO - ITE
  • ATLAS - ITE
  • ATLAS PLUS - ITE
  • COMMUNICARE
  • DIGIFOCUS
  • DIGIFOCUS II - ITE
  • DIGILIFE
  • DIGILIFE.COM - ITE
  • EPOQ W - ITE
  • EPOQ XW - ITE
  • EPOQV ITE
  • ERGO - ITE
  • GAIA - ITE
  • GET - ITE
  • GO - ITE
  • GO PRO - ITE
  • HIT - ITE
  • HIT PRO- ITE
  • INO - ITE
  • INO PRO - ITE
  • INTIGAI - ITE
  • MICROFOCUS
  • MONARCH ITE
  • MULTIFOCUS
  • NERA - ITE
  • NERA 2 ITE
  • NERA 2 PRO ITE
  • NERA PRO - ITE
  • O2 - ITE
  • O2 PRO - ITE
  • OPN
  • PRIMOFOCUS
  • RIA - ITE
  • RIA 2 ITE
  • RIA 2 PRO ITE
  • RIA PRO - ITE
  • SAFRAN ITE
  • SIYA
  • SYNCRO ITE
  • TEGO ITC
  • TEGO ITE
  • TEGO PRO ITC
  • TEGO PRO ITE
  • VIGO CONNECT ITE
  • VIGO ITE
  • VIGO PRO CONNECT ITE
  • VIGO PRO ITE

Recalls and safety alerts that mention it

Health Canada’s recall notices do not carry licence numbers, so these are matched by name: notices whose title or product names “in-the-ear”. A notice may cover another product or only some lots: read it to see what it covers.

Class I devices, the lowest-risk group, mostly need no device licence, so most are not in this list.