MedtechSourcebook

ORCHID ORTHOPEDIC SOLUTIONS LANSING

Contract manufacturer ยท Holt, MI

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

2025Product codes first listed, by year (tallest: 2)2026
FDA registration
3005852519 (openFDA record; or search FDA's registration database)
FEI number
3005852519
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
ORCHID ORTHOPEDIC SOLUTIONS LLC (FDA owner/operator no. 9085942)
Registered address
1489 CEDAR ST., Holt, MI 48842
Contract listings
3 device listings, 3 product codes, first listed May 20, 2025
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/PolymerClass IIOrthopedicContract manufacturingApr 13, 2026
LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous UncementedClass IIOrthopedicContract manufacturingJun 4, 2026
MBHProsthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/PolymerClass IIOrthopedicContract manufacturingMay 20, 2025