HOAClass I
Compressor, Orbital
Ophthalmic · 21 CFR 886.4350
MDR events10All time
Recalls0All time
Registered firms6Currently listed
510(k) clearances0All time
Recent MDR events
10 adverse event reports on file
- CUSTOMEYESSep 15, 2022InjuryBeaver Visitec International Limited3002808441-2022-00001
- DAVIS BRAIN SPATULA MALL 178X26MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00031
- DAVIS BRAIN SPATULA MALL 178X16MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00034
- DAVIS BRAIN SPATULA MALL 178X13MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00033
- DAVIS BRAIN SPATULA MALL 178X9MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00030
- DAVIS BRAIN SPATULA MALL 178X19MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00032
- DAVIS BRAIN SPATULA MALL 178X6MMJan 28, 2020MalfunctionAesculap Inc2916714-2020-00029
- BA-320-185Sep 8, 2014MalfunctionBiotex, Inc.3005726841-2014-00008
- BA-320-185Aug 27, 2014MalfunctionBiotex Medical3005726841-2014-00007
- BA-320-185Jul 23, 2014Malfunction3005726841-2014-00006
Event type breakdown
Malfunction9
Injury1
Most-reported manufacturers
Recalls
0 recall events for this product code
No recalls on file for this product code.
Registered firms
6 firms currently registered for this product code
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for this product code.