Data / Medical devices / United States / Meddev Corp.
Meddev Corp.: FDA-registered device maker in Sunnyvale, CA, United States, 3 510(k) clearances
Meddev Corp. is registered with the FDA (registration 2921577) in Sunnyvale, CA, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated August 17, 2015. 1 recall event names it as the recalling firm. 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
- 2921577
- Address
- 730 North Pastoria Ave., Sunnyvale, CA, United States, 94085
- Owner or operator
- MEDDEV CORP. (2921577)
- Roles
- Manufacturer
- First device listed
- November 7, 1977
- Registered through
- 2026
- Brand names listed
- " "MEDDEV SURGICAL HEADL, Blinkeze External Eyelid Weight, Contour, EyeClose Adhesive Strips, SAME (OR "MEDDEV SURGICAL HEADLIGHT, THE HAND HELPER, Tantalum Eyelid Weight Sizing Set, ThinProfile
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Exerciser, Non-Measuring | ION | 1 | Manufacturer | accessdata.fda.gov |
| Light, Surgical Headlight | EBA | 1 | Manufacturer | accessdata.fda.gov |
| Weights, Eyelid, External | MML | 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 |
|---|---|---|---|---|---|---|
| August 17, 2015 | K150986 | Contour Eyelid Weight Implants, ThinProfile Eyelid Weight Implants | MML | Substantially Equivalent | Meddev Corporation | accessdata.fda.gov |
| July 2, 2001 | K011740 | CONTOUR DESIGN GOLD EYELID IMPLANT, MODEL CONTOUR DESIGN (SERIES 3000) | MML | Substantially Equivalent | Meddev Corp. | accessdata.fda.gov |
| June 8, 1994 | K940974 | EYECLOSE EXTERNAL EYELID WEIGHTS | MML | Substantially Equivalent | Meddev Corp. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| July 12, 2024 | 96551 | Class II | Ongoing | Brand Name: Contour Product Name: Contour Gold Eyelid Weight Model/Catalog Number: LL3010 Product Description: Contour Gold Eyelid Weight, 1.0 gm MedDev Contour and ThinProfile Eyelid Weight Implants are designed for the | Due to mislabeling of products | accessdata.fda.gov |
Compare with other makers
- All makers of Weights, Eyelid, External
- All makers of Exerciser, Non-Measuring
- All makers of Light, Surgical Headlight
Updated May 9, 2025. 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.