BISHOP

FDA Device Registration & Listing · Shreveport, LA, US · Registration 3017926429

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
3017926429
FEI Number
3017926429
Entity Name
BISHOP
City/State/Country
Shreveport, LA, US
Establishment Address
415 Texas St Ste 310, Shreveport, LA 71101, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Bishop (Owner Number: 10080093)
Owner / Operator Contact Address
717 Crockett St, Suite 205, Shreveport, LA 71101, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Bishop Aegis

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2021-01-12

Official Correspondent

Eric Rippetoe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017926429. Last updated year: 2026. Please use registration number 3017926429 when referencing this establishment in official correspondence.
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