HXDClass I

Clamp

21 CFR 878.4800 / General, Plastic Surgery

HXD is the FDA product code for Clamp, a class I device type, regulated under 21 CFR 878.4800. As of 2026-09-10, FDA records hold 14 510(k) clearances under this code, the most recent dated 1989-02-03, and 4 recalls.

Classification record

Product code: HXD
Device name: Clamp
Regulation: 21 CFR 878.4800
Device class: Class I
Review panel: General, Plastic Surgery
Submission type: 510(k) exempt
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 14
Ingested recalls: 4

Clearances, product code HXD

By decision year

14 clearances under product code HXD with a decision year between 1977 and 1989, 1989 the highest year at 4.

Show the numbers

510(k) clearances under FDA product code HXD by decision year
Year	Clearances
1977	1
1978	1
1979	1
1980	2
1985	2
1986	1
1987	2
1989	4

Applicants with the most clearances

Product code HXD

Applicants holding the most 510(k) clearances under product code HXD
Applicant	Clearances
Kinetic Medical Products	4
Robert I. Chien & Assoc., Inc.	2
B & B Medical Technologies, Inc.	1
Concord Laboratories, Inc.	1
Cp Medical	1
Hemoy, Inc.	1
Med-Tool, Inc.	1
Omni Intl., Inc.	1
Solway, Inc.	1
Stryker Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 311 companies shown, in name order