BIOS

FDA Device Registration & Listing · Nesbit, MS, US · Registration 3033273230

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3033273230
FEI Number
3033273230
Entity Name
BIOS
City/State/Country
Nesbit, MS, US
Establishment Address
1295 Nesbit Drive, Nesbit, MS 38651, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
BIOS (Owner Number: 10091714)
Owner / Operator Contact Address
1295 Nesbit Drive, Nesbit, MS 38651, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Catalyst R1 Reverse Shoulder System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented Orthopedic Class 2 888.3690 2024-10-27
PHX Shoulder Prosthesis, Reverse Configuration Orthopedic Class 2 888.3660 2024-10-27

Official Correspondent

Carey Bryant

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BIOS
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K984202 Howmedica, Inc. HOWMEDICA HUMERAL INTERCALARY SYSTEM 1999-02-05
K141345 Tornier S.A.S. AEQUALIS FX2 2014-11-18

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3033273230. Last updated year: 2026. Please use registration number 3033273230 when referencing this establishment in official correspondence.
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