Ryder Contact Lens Case
by Bradstreet Clinical Research Assoc., Inc.
510(k) K951181
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK951181 | Date12 May 1995 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- LRX
- Device Class
- Class II
- Regulation
- 21 CFR Part 886.5928
- Advisory Committee
- Ophthalmic
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 21 Sep 2026
The Ryder Contact Lens Case is a medical device classified as a contact lens case. It is designed to provide a storage environment for contact lenses.
This device is regulated under FDA 510(k) clearance K951181. It is categorized as a class 2 medical device within the ophthalmic specialty.
Other devices from Bradstreet Clinical Research Assoc., Inc.
Questions
AI-generated answers, 21 Sep 2026
What is the primary purpose of the Ryder Contact Lens Case?
The Ryder Contact Lens Case is designed to provide a dedicated storage environment for contact lenses, ensuring they are held securely when not in use.
Is this device regulated by the FDA?
Yes, the Ryder Contact Lens Case is a class 2 medical device that has received FDA 510(k) clearance under the number K951181.
Which medical specialty does this device fall under?
This device is categorized within the ophthalmic specialty, as it is specifically engineered for the storage of contact lenses.