FDA device listing
GYNECARE TVT ABBREVO Continence System
FDA device listing 1936972160 · ETHICON INC.
Key facts
| Proprietary names | GYNECARE TVT ABBREVO Continence System |
|---|---|
| Owner/operator | ETHICON INC. |
| Owner/operator number | 2210968 |
| Premarket submissions | K100936 |
| Product codes | OTN |
| Device names | OTN - Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.3300 |
| Review panels | General & Plastic Surgery |
| Registered establishments | ETHICON SARL, GMED Healthcare BVBA ( a Johnson & Johnson Company) |
| Establishment registrations | 3003702646, 3014272734 |
| FEI numbers | 3003702646, 3014272734 |
| Establishment operations | Contract Manufacturer, Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database