Data / Medical devices / United States / Benz Research And Development LLC
Benz Research And Development LLC: FDA-registered device maker in Sarasota, FL, United States, 7 510(k) clearances
Benz Research And Development LLC is registered with the FDA (registration 1052446) in Sarasota, FL, United States. It lists 1 device type. The FDA files 7 510(k) clearances under its listings, the newest dated August 9, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1052446
- FEI number
- 1000027288
- Address
- 6447 Parkland Dr, Sarasota, FL, United States, 34243
- Owner or operator
- BENZ RESEARCH AND DEVELOPMENT LLC (9007059)
- Roles
- Contract manufacturer, Contract sterilizer, Manufacturer
- First device listed
- November 13, 2007
- Registered through
- 2026
- Brand names listed
- BENZ G3X, BENZ G4X, BENZ G5X, BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS, Benz 38, Benz G 5X, Benz Methafilcon, Extreme H2O
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lenses, Soft Contact, Daily Wear | LPL | 2 | Contract manufacturer, Contract sterilizer, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 9, 2010 | K101122 | BENZ-G 4X (HIOXIFILCON D) MULTIFOCAL LATHED LENS | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| August 6, 2007 | K062854 | BENZ-G 4X HIOXIFILCON D | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| March 8, 2001 | K003861 | BENZ-MF (VISIBILITY HANGLING TINT) (METHAFILCON A) SOFT DAILY WEAR CONTACT LENS (LATHE-CUT) | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| December 22, 1998 | K983773 | BENZ G-5X (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| February 27, 1998 | K980418 | BENZ METHAFILCON A OPTICAL BLANK, BENZ METHAFILCON A SPHERICAL AND TORIC SOFT (HYDROPHILIC) CONTACT LENSES FOR DAILY WER | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| March 7, 1997 | K964528 | (LENSES) BENZ-G 3X (HIOXIFILCON B) SPHERICAL AND TORIC SOFT (HYDROPHILIC) CONTACT LENSES IN CLEAR AND WITH A BLUE TINT | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
| August 23, 1996 | K961103 | BENZ 38 CLEAR & WITH BLUE VISIBILITY TINT | LPL | Substantially Equivalent | Benz Research and Development Corp. | accessdata.fda.gov |
Compare with other makers
Updated August 9, 2010. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.