Data / Medical devices / United Kingdom / Cantor Barnard Ltd
Cantor Barnard Ltd: FDA-registered device maker in Northamptonshire, United Kingdom, 7 510(k) clearances
Cantor Barnard Ltd is registered with the FDA (registration 9610790) in Northamptonshire, United Kingdom. It lists 4 device types. The FDA files 7 510(k) clearances under its listings, the newest dated October 26, 2004. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 9610790
- FEI number
- 3002807717
- Address
- Market Place, Brackley, Northamptonshire, United Kingdom, NN13 7DP
- Owner or operator
- CANTOR BARNARD LTD (8010037)
- Roles
- Manufacturer
- First device listed
- May 28, 1992
- Registered through
- 2026
- Brand names listed
- Cantor Cosmetic, Cantor Prosthetic, ChromaGen, Nissel Custom, Zero 6
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Eye, Artificial, Non-Custom | HQH | 1 | Manufacturer | accessdata.fda.gov |
| Lens, Contact, For Color Vision Deficiency | NCZ | 2 | Manufacturer | accessdata.fda.gov |
| Lens, Contact, For Reading Discomfort | NIC | 2 | Manufacturer | accessdata.fda.gov |
| Lenses, Soft Contact, Daily Wear | LPL | 2 | 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 |
|---|---|---|---|---|---|---|
| October 26, 2004 | K042435 | COOPER PROSTHETIC | LPL | Substantially Equivalent | CooperVision, Inc. | accessdata.fda.gov |
| July 30, 2004 | K041700 | CANTOR & NISSEL HAND PAINTED PROSTHETIC SOFT CONTACT LENS FOR DAILY WEAR | LPL | Substantially Equivalent | Cantor & Nissel , Ltd. | accessdata.fda.gov |
| May 9, 2002 | K012132 | CHROMAGEN V3.0 READING AID SOFT CONTACT LENS | NIC | Substantially Equivalent | Cantor & Nissel , Ltd. | accessdata.fda.gov |
| October 20, 2000 | K994320 | CHROMAGEN V2.0 HAPLOSCOPIC SYSTEM & COLOR VISION ENHANCEMENT SOFT CONTACT LENSES | NCZ | Substantially Equivalent | Cantor & Silver , Ltd. | accessdata.fda.gov |
| August 18, 1999 | K992500 | CANTOR & SILVER 5X PROSTHETIC TINTED (HIOXIFILCON A) SOFT DAILY WEAR CONTACT LENS | LPL | Substantially Equivalent | Cantor & Silver , Ltd. | accessdata.fda.gov |
| April 21, 1999 | K990757 | CANTOR & SILVER 5X TINTED (HIOXIFILCON A) SOFT (SPHERICAL & TORIC) DAILY WEAR CONTACT WEAR CONTACT LENS, TINTED (TRANSPA | LPL | Substantially Equivalent | Cantor & Silver , Ltd. | accessdata.fda.gov |
| June 24, 1998 | K981779 | CANTOR & SILVER 5X (HIOXIFILCON A) SOFT (SPHERICAL & TORIC) DAILY WEAR CONTACT LENS (CLEAR & BLUE VISIBILITY TINTED, LAT | LPL | Substantially Equivalent | Cantor & Silver , Ltd. | accessdata.fda.gov |
Compare with other makers
Updated October 26, 2004. 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.