FDA device listing
[SL-700-32] Humby Dermatome / Skin Graft Knife 32 cm - 13 Stainless Steel,[SL-710-30] Watson Dermatome / Skin Graft…
FDA device listing 1430295253 · Surtex Instruments Ltd
Key facts
| Proprietary names | [SL-700-32] Humby Dermatome / Skin Graft Knife 32 cm - 13 Stainless Steel,[SL-710-30] Watson Dermatome / Skin Graft Knife 30.5 cm - 12 Stainless Steel,[SL-712-00] Dermatome Blade Box of 10 for SL-700-32 and SL-710-30 15 cm - 6 Stainless Steel,[SL-722-00] Blades for Large Humby Dermatome with 4 Holes (Pack of 10),[SL-730-31] Schink Dermatome / Skin Graft Knife Adjustable From 0.1 to 2.0 mm 31 cm… |
|---|---|
| Owner/operator | Surtex Instruments Ltd |
| Owner/operator number | 10061887 |
| Product codes | GFD |
| Device names | GFD - Dermatome |
| Device class | Class I |
| Classification regulations (21 CFR) | 878.4820 |
| Review panels | General & Plastic Surgery |
| Registered establishments | SURTEX INSTRUMENTS LTD |
| Establishment registrations | 3016069968 |
| FEI numbers | 3016069968 |
| Establishment operations | Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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