VILET
GUDID 10812444023340
SUTURE
RIVERPOINT MEDICAL, LLC
Polyester suture, bioabsorbable, multifilament| Primary Device ID | 10812444023340 |
| NIH Device Record Key | d22186d5-d1a1-4c5b-8791-f5b5abe7ac95 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VILET |
| Version Model Number | V392 |
| Company DUNS | 964053560 |
| Company Name | RIVERPOINT MEDICAL, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00812444023343 [Primary] |
| GS1 | 10812444023340 [Package] Contains: 00812444023343 Package: [12 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K120556
FDA Product Code
| GAM | Suture, Absorbable, Synthetic, Polyglycolic Acid |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-10-14 |
| Device Publish Date | 2016-11-17 |
On-Brand Devices [VILET]
Trademark Results [VILET]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 VILET 85392464 4114966 Live/Registered |
RIVERPOINT MEDICAL, LLC 2011-08-08 |
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