RELIGN CORPORATION

FDA Device Registration & Listing · Santa Clara, CA, US · Registration 3012790575

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
3012790575
FEI Number
3012790575
Entity Name
RELIGN CORPORATION
City/State/Country
Santa Clara, CA, US
Establishment Address
1725 De La Cruz Blvd Ste 7, Santa Clara, CA 95050, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
RELIGN Corporation (Owner Number: 10053774)
Owner / Operator Contact Address
1725 De La Cruz Blvd Ste 7, Santa Clara, CA 95050, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K233493
PMA Number
N/A

All Registered Proprietary Names

Relign Arthroscopic System Tricera

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-01-10
HRX Arthroscope Orthopedic Class 2 888.1100 2017-01-10
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2024-02-06
HRX Arthroscope Orthopedic Class 2 888.1100 2024-02-06

Official Correspondent

Michael Duvall

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

RELIGN Corporation
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
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0041-05 Linvatec Corp. 2
Ultra Power Burs, Sterile, Single-Use.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3012790575. Last updated year: 2026. Please use registration number 3012790575 when referencing this establishment in official correspondence.
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