Magnivision, Inc.
United StatesFDA applicant, unverified
- Devices
- 8
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Magnivision, Inc. makes
Magnivision, Inc. manufactures accessories for contact lens care, including hard and soft contact lens holders, contact lens cases, and tools for removing lenses. Products include specialized holders like the DELUXE CONTACT LENS HOLDER, reusable and single-use lens cases (e.g., MAGNIF-EYES, CONFEES+, COMFEES+ CON-PAK), and dedicated lens removal devices for both hard and soft lenses.
The company’s portfolio is regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. Products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Deluxe Contact Lens Holder (Hard & Soft) #283 Ref K882384
Regimes: 510(k) Registry: 510(k)Item #352/#CS352* Contact Lens Cases Ref K890533
Regimes: 510(k) Registry: 510(k)Soft Contact Lens Remover Ref K872567
Regimes: 510(k) Registry: 510(k)Item #272 Magnif-Eyes Contact Lens Case Ref K900778
Regimes: 510(k) Registry: 510(k)Confees(R)+ Contact Lens Holder Ref K897084
Regimes: 510(k) Registry: 510(k)Item #273 Contact Lens Cases Ref K900777
Regimes: 510(k) Registry: 510(k)Comfees(R) + Con-Pak(Tm) Lens Case Ref K897085
Regimes: 510(k) Registry: 510(k)Hard Contact Lens Remover. Item #289 Ref K872591
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by Magnivision, Inc., initiated on 2003-05-02. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2003
- 2 May 2003 Z-0541-04 Unclassified (pre-2012) Terminated Possibility of eye injury from large temple tags on promotional sale product when customer tries them on in store.
Frequently asked questions
How many devices does Magnivision, Inc. have in the registry?
The registry currently lists 8 devices for Magnivision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Magnivision, Inc.'s devices?
Among its 8 most recently registered devices, Magnivision, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do Magnivision, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for Magnivision, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Magnivision, Inc.?
FDA recall records list 1 recall initiated by Magnivision, Inc., the most recent initiated on 2 May 2003. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Magnivision, Inc. in the registry?
The most recently registered devices listed for Magnivision, Inc. include DELUXE CONTACT LENS HOLDER (HARD & SOFT) #283, ITEM #352/#CS352* CONTACT LENS CASES, SOFT CONTACT LENS REMOVER and ITEM #272 MAGNIF-EYES CONTACT LENS CASE.