Landers Silicone Vitrectomy Lens Ring
Catalogue number OLV-1S, listed by Ocular Instruments, Inc., United States, under Ring, Ophthalmic (Flieringa). 3 manufacturers in China are registered for this product code.
3manufacturers in China registered for this device type
1catalogue number
5510(k) clearances naming this product code
Who Else Makes It
All of them in Jiangsu.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| 66 Vision Tech Co., Ltd. | Suzhou | Jiangsu | Private-label distributor | 24 |
| Huaian Tisurg Medical Instruments Co., Ltd. | Huaian | Jiangsu | Contract manufacturer | 22 |
| Belle Healthcare Technology Co., Ltd. | Suzhou | Jiangsu | Manufacturer | 20 |
Record
| Listed by | Ocular Instruments, Inc., United States |
|---|---|
| FDA product code | HNH |
| Device type | Ring, Ophthalmic (Flieringa) |
| Device class | Class 1 |
| Regulation | 21 CFR 886.4350 |
| Establishment | Manufacturer |
| 510(k) | K912269 |
| Record published | 2019-06-11 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| OLV-1S | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Ambler Surgical | Ambler Surgical, LLC | 96 |
| MR Phaco | Crestpoint Management Ltd. | 52 |
| Millennium | Avalign Technologies, Inc. | 21 |
| Bausch + Lomb | Bausch & Lomb Incorporated | 17 |
| MSI Precision Specialty Instruments | MED Saver, Inc. | 15 |
| Stephens Instruments | Krishna Imports Inc | 15 |
| Ophthalmic Ring | Katena Products, Inc. | 13 |
| Wexler Surgical, Inc. | Wexler Surgical, Inc. | 13 |
| Aesculap | Aesculap AG | 12 |
| Ring, Ophthalmic (Flieringa) | Geuder Aktiengesellschaft | 11 |
| Symmetry Surgical | Aspen Surgical Products, Inc. | 9 |
| Rumex | Rumex International Co. | 9 |
Showing 12 of 98. All products under Ring, Ophthalmic (Flieringa)
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K912268 | 1991-08-07 |
| K912269 | 1991-08-07 |
| K912151 | 1991-07-25 |
| K902496 | 1990-07-24 |
| K850991 | 1985-03-29 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.