Unilens Corp., USA
Unilens Corp., USA holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2014.
Top product codes for Unilens Corp., USA
Recent clearances by Unilens Corp., USA
- K142851 — CVue ADVANCED (hioxifilcon D) Soft (hydrophilic) Contact Lens
- K121652 — CVUE ADVANCED HYDRA VUE
- K110452 — SOF-FORM II, UNILENS, UNISITE, SIMULVUE, AQUAFLEX, LL-38, BAYVUE AQUAFLEX MTO, UNILENS 38, UNISOFT, SIMULVUE 38 LLBI 2,
- K100456 — CVUE ADVANCED DEFINITIVE
- K082393 — CVUE ADVANCED (HIOXIFILCON D) SOFT (HYDROPHILIC) CONTACT LENS
- K050743 — AQUAFLEX 2 (TEFILCON) CONTACT LENS
- K041608 — C-VUE 55 TORIC (METHAFILCON A) MULTIFOCAL CONTACT LENS
- K002408 — AXION PLUS (METHAFILCON A) SOFT (HYDROPHILIC) ASPHERIC CONTRACT LENS
- K960926 — POWER PLUS (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
- K960376 — FREESOFT (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
- K960380 — SEESOFT (POLYMACON) SOFT (HYDROPHILIC) ASPHERIC CONTACT LENS
- K941836 — UNILENS 38 SOFT ASPHERIC CONTACT LENS
- K942372 — SIMULVUE 38 (POLYMACON) SOFT (HYDROPHILIC) BIFOCAL CONTACT LENS
- K940777 — BAYVUE (POLYMACON) SOFT (HYDROPHILIC) CONTACT LENS
Data sourced from openFDA. This site is unofficial and independent of the FDA.