Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Meddev Corp with 3 510(k) clearances and 2 device recalls. The most recent is a device recall dated Jul 12, 2024: Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 12, 2024 | Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3012 Product Description: Contour Gold Eyelid WeightClass II · Due to mislabeling of products | Device recalls |
| Jul 12, 2024 | Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid WeightClass II · Due to mislabeling of products | Device recalls |
| Aug 17, 2015 | Contour Eyelid Weight Implants, ThinProfile Eyelid Weight ImplantsK150986 · MML | 510(k) clearances |
| Jul 2, 2001 | CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000)K011740 · MML | 510(k) clearances |
| Jun 8, 1994 | EYECLOSE EXTERNAL EYELID WEIGHTSK940974 · MML | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
