NAAClass IIIImplant
Lens, Intraocular, Accommodative
Ophthalmic · 21 CFR 886.3600
MDR events1,402All time
Recalls1All time
Registered firms4Currently listed
510(k) clearances0All time
Recent MDR events
1,402 adverse event reports on file
- CRYSTALENSJan 2, 2026OtherBausch&lomb IncorporatedMW5181593
- CRYSTALENS ACCOMMODATING IOLJul 25, 2024InjuryBausch + Lomb0001313525-2024-00128
- CRYSTALENS ACCOMMODATING IOLSep 1, 2023InjuryBausch + Lomb0001313525-2023-70104
- CRYSTALENS ACCOMMODATING IOLSep 1, 2023InjuryBausch + Lomb0001313525-2023-70105
- CRYSTALENS ACCOMMODATING IOLDec 22, 2022InjuryBausch + Lomb0001313525-2022-00189
- INTRAOCULAR LENS FOR POSTERIOR CHAMBER CRYSTALENSOct 25, 2022InjuryBausch And Lomb IncorporatedMW5112851
- NAAug 11, 2022MalfunctionZoll Manufacturing Corporation3008642652-2022-22029
- CRYSTALENS ACCOMMODATING IOLJul 7, 2022InjuryBausch + Lomb0001313525-2022-00090
- CRYSTALENS ACCOMMODATING IOLApr 27, 2022InjuryBausch + Lomb0001313525-2022-00048
- CRYSTALENS ACCOMMODATING IOLMar 15, 2022InjuryBausch + Lomb0001313525-2022-00029
Event type breakdown
Injury1,382
Malfunction15
Unspecified3
Other2
Recalls
1 recall events for this product code
Registered firms
4 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.
PMA approvals
1 premarket approvals for this product code