Atlas FDA

HXD

14 FDA 510(k) clearances · Product code

14 daysmedian time to decision
28 days90th percentile
14clearances measured

FDA profile

Official device name
Clamp
Device class
Class I (low risk)
Regulation
21 CFR 878.4800
Medical specialty
General, Plastic Surgery
Adverse events (MAUDE)
2021: 75 · 2022: 88 · 2023: 99 · 2024: 135 · 2025: 124 · 2026: 76
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
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RecordFirmDate
KIDNEY CLAMP (K890368)Kinetic Medical Products1989-02-03
INTESTINAL CRUSHING CLAMP (K890371)Kinetic Medical Products1989-02-03
INTESTINAL CLAMP (K890372)Kinetic Medical Products1989-02-03
PARAMETRIUM CLAMP (K890381)Kinetic Medical Products1989-02-03
VASCULAR CLAMP (K874959)Solway, Inc.1987-12-30
C CLAMP (K872386)Med-Tool, Inc.1987-07-02
SUCTION-OFF (K863653)B&B Medical Technologies, Inc.1986-10-07
CANNULA CLAMP (K853538)Cp Medical1985-09-12
OMNIMED CLAMP (K851654)Omni Intl., Inc.1985-05-31
SURGICAL INSTRUMENTS (K801819)Robert I. Chien & Assoc., Inc.1980-08-20
RICA OR SMIC SURGICAL INSTRUMENTS (K801028)Robert I. Chien & Assoc., Inc.1980-05-20
GIZMO TOWEL CLAMP (K791289)Hemoy, Inc.1979-07-24
CLAMP, DISPOSABLE (K782090)Concord Laboratories, Inc.1978-12-20
CARPENTER BONE CLAMP (K770118)Stryker Corp.1977-01-26

Track HXD automatically

Every clearance here is in the API, with alerts when new ones post.