FDA device listing
Deklene,DEKNATEL,MULTIPLE STERILE ABSORABLE SUTURES,OPTHAMEND
FDA device listing 1073682262 · Teleflex
Key facts
| Proprietary names | Deklene,DEKNATEL,MULTIPLE STERILE ABSORABLE SUTURES,OPTHAMEND |
|---|---|
| Owner/operator | Teleflex |
| Owner/operator number | 9062981 |
| Premarket submissions | K930738 |
| Product codes | GAL, GAM, GAP, GAQ, GAR, GAT, GAW |
| Device names | GAL - Suture, Absorbable, Natural, GAM - Suture, Absorbable, Synthetic, Polyglycolic Acid, GAP - Suture, Nonabsorbable, Silk, GAQ - Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile, GAR - Suture, Nonabsorbable, Synthetic, Polyamide, GAT - Suture, Nonabsorbable, Synthetic, Polyethylene, GAW - Suture, Nonabsorbable, Synthetic, Polypropylene |
| Device class | Class II |
| Classification regulations (21 CFR) | 878.4493, 878.4495, 878.4830, 878.5000, 878.5010, 878.5020, 878.5030 |
| Review panels | General & Plastic Surgery |
| Registered establishments | Teleflex LLC (NADC), Teleflex Medical de Mexico, S. de R.L. de C.V., Teleflex Medical LLC |
| Establishment registrations | 3004365956, 3010041511, 3011137372 |
| FEI numbers | 3004365956, 3005747797, 3010041511 |
| Establishment operations | Complaint File Establishment, Specification Developer, Manufacturer, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None 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