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

Bender

21 CFR 888.4540 / Orthopedic
FDA source (opens on fda.gov)

HXW is the FDA product code for Bender, a class I device type, regulated under 21 CFR 888.4540. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and 3 recalls.

Classification record

Product code
HXW
Device name
Bender
Regulation
21 CFR 888.4540
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
3
Ingested recalls
3

Clearances, product code HXW

By decision year
3 clearances under product code HXW with a decision year between 1987 and 1987, 1987 the highest year at 3.
Show the numbers
510(k) clearances under FDA product code HXW by decision year
YearClearances
19873

Applicants with the most clearances

Product code HXW
Applicants holding the most 510(k) clearances under product code HXW
ApplicantClearances
Buckman Co., Inc.1
Military Engineering, Inc.1
Terray Manufacturing, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 210 companies shown, in name order