510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K955170Substantially Equivalent

Nexflex Femoral Stem, Standard Design

Nexmed, Inc., Palm Desert CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K955170 is the FDA 510(k) clearance record for NEXFLEX FEMORAL STEM, STANDARD DESIGN, a class II device, cleared for Nexmed, Inc. on under FDA product code LPH (Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented). FDA records list 6 510(k) clearances for Nexmed, Inc., from to . As of , FDA records show no recalls naming K955170.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented
Regulation
21 CFR 888.3358
Device class
Class II
Review panel
Orthopedic
Applicant
Nexmed, Inc. 42-160 State St., Palm Desert CA
510(k) summary
Summary
Third party review
No

Clearances, product code LPH

Trailing 12 months
11 clearances under product code LPH in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code LPH, trailing twelve months
MonthClearances
November 20252
December 20251
January 20261
February 20261
March 20260
April 20260
May 20261
June 20261
July 20261
August 20262
September 20261
October 20260