Product code HXD— General, Plastic Surgery
C CLAMP
- Classification name
- Clamp
- Device class
- Class 1
- Regulation
- 21 CFR 878.4800
- Advisory panel
- General, Plastic Surgery
- Total cleared
- 14
- First cleared
- Most recent
Market context for product code HXD
FDA has cleared devices under product code HXD between 1977 and 1989, filed by 10 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
- 1989
- 1987
- 1986
- 1985
- 1980
- 1979
- 1978
- 1977
Top applicants under product code HXD
Adverse events under product code HXD
product code HXD- Malfunction
- 660
- Total
- 660
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 HXD
- K890368 — KIDNEY CLAMP
- K890371 — INTESTINAL CRUSHING CLAMP
- K890372 — INTESTINAL CLAMP
- K890381 — PARAMETRIUM CLAMP
- K874959 — VASCULAR CLAMP
- K872386 — C CLAMP
- K863653 — SUCTION-OFF
- K853538 — CANNULA CLAMP
- K851654 — OMNIMED CLAMP
- K801819 — SURGICAL INSTRUMENTS
- K801028 — RICA OR SMIC SURGICAL INSTRUMENTS
- K791289 — GIZMO TOWEL CLAMP
- K782090 — CLAMP, DISPOSABLE
- K770118 — CARPENTER BONE CLAMP
Data sourced from openFDA. This site is unofficial and independent of the FDA.