Product code GDT— General, Plastic Surgery
3M DISPOSABLE SKIN STAPLER
- Classification name
- Staple, Removable (Skin)
- Device class
- Class 1
- Regulation
- 21 CFR 878.4760
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 19
- First cleared
- Most recent
Market context for product code GDT
FDA has cleared devices under product code GDT between 1976 and 1996, filed by 15 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.
Clearances per year
- 1996
- 1994
- 1993
- 1992
- 1991
- 1990
- 1986
- 1985
- 1984
- 1983
- 1982
- 1980
- 1976
Top applicants under product code GDT
Adverse events under product code GDT
product code GDT- Malfunction
- 752
- Total
- 752
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code GDT
- K963234 — STAPLE REMOVAL KIT
- K943719 — VISISTAT STAPLER
- K925526 — MANIPLER DISPOSABLE SKIN STAPLER
- K915430 — SKIN STAPLE REMOVER KIT
- K911204 — QUALTEX SKIN STAPLE EXTRACTOR
- K910586 — AUTO SUTURE(R) POLYMER SKIN GRAFT STAPLER*
- K900486 — APPOSE UNITY STERILE DISPOSABLE SKIN STAPLER
- K861711 — SKIN STAPLE REMOVER WITH SPONGE STERILE DISPOSABLE
- K851974 — V. MUELLER VITAL SKIN STAPLER
- K844837 — VISISTAT SKIN STAPLING DEVICE
- K844838 — SKIN STAT II SKIN STAPLING MEDICAL DEVICE
- K833085 — STAPLE REMOVER SR300P
- K833357 — VYDAX 525-550 & 5100 FLUOROTELOMER
- K832709 — SKIN STAPLING DEVICE SC2000
- K822365 — CENTURION SKIN STAPLE REMOVER
- K821024 — DISP. SKIN STAPLER REMOVALBLE SKINSTAPLE
- K801444 — SKIN STAPLE REMOVER #523770
- K800535 — 3M DISPOSABLE SKIN STAPLER
- K760734 — REGULAR AND WIDE SKIN STAPLES
Data sourced from openFDA. This site is unofficial and independent of the FDA.