SUTUREGARD MEDICAL, INC.

FDA Device Registration & Listing · Corvallis, OR, US · Registration 3015045268

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
3015045268
FEI Number
3015045268
Entity Name
SUTUREGARD MEDICAL, INC.
City/State/Country
Corvallis, OR, US
Establishment Address
257 SW Madison Avenue Suite 210, Corvallis, OR 97333, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SUTUREGARD Medical, Inc. (Owner Number: 10058863)
Owner / Operator Contact Address
4640 S Macadam Ave, Portland, OR 97239, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

HEMIGARD Interlock HEMIGARD ADHESIVE RETENTION SUTURE DEVICE SUTUREGARD INTRAOPERATIVE SKIN RELAXATION RETENTION SUTURE DEVICE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MKY System, Skin Closure General, Plastic Surgery Class 1 878.4320 2022-09-30
KGS Retention Device, Suture General, Plastic Surgery Class 1 878.4930 2018-11-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SUTUREGARD Medical, Inc.
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 3015045268. Last updated year: 2026. Please use registration number 3015045268 when referencing this establishment in official correspondence.
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