HTDClass I

Forceps

21 CFR 878.4800 / General, Plastic Surgery

HTD is the FDA product code for Forceps, a class I device type, regulated under 21 CFR 878.4800. As of 2026-09-10, FDA records hold 73 510(k) clearances under this code, the most recent dated 2005-09-08, and 14 recalls.

Classification record

Product code: HTD
Device name: Forceps
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: 73
Ingested recalls: 14

Clearances, product code HTD

By decision year

73 clearances under product code HTD with a decision year between 1977 and 2005, 1984 the highest year at 18.

Show the numbers

510(k) clearances under FDA product code HTD by decision year
Year	Clearances
1977	3
1980	2
1982	3
1983	2
1984	18
1985	11
1987	13
1989	15
1991	2
1998	3
2005	1

Applicants with the most clearances

Product code HTD

Applicants holding the most 510(k) clearances under product code HTD
Applicant	Clearances
Imm Enterprises, Ltd.	14
Kinetic Medical Products	14
The Huxley Instrument Corp.	9
Arthropedics, Inc.	8
Titan Mfg., Inc.	3
Almore Intl., Inc.	2
Artiberia	2
Cimed Intl., Inc.	2
Conphar, Inc.	2
Solway, Inc.	2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 637 companies shown, in name order