510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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HTCClass I

Pliers, Surgical

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

HTC is the FDA product code for Pliers, Surgical, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 10 510(k) clearances under this code, the most recent dated , and 4 recalls.

Classification record

Product code
HTC
Device name
Pliers, Surgical
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
10
Ingested recalls
4

Clearances, product code HTC

By decision year
10 clearances under product code HTC with a decision year between 1983 and 1987, 1984 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code HTC by decision year
YearClearances
19831
19845
19851
19862
19871

Applicants with the most clearances

Product code HTC
Applicants holding the most 510(k) clearances under product code HTC
ApplicantClearances
Med-Tool, Inc.9
The Anspach Effort, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 232 companies shown, in name order