OSHERU, Inc.

FDA Device Registration & Listing · Bend, OR, US · Registration 3026790897

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
3026790897
FEI Number
3026790897
Entity Name
OSHERU, Inc.
City/State/Country
Bend, OR, US
Establishment Address
1901 NW Rivermist Dr., Bend, OR 97703, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Osheru (Owner Number: 10087597)
Owner / Operator Contact Address
1901 NW Rivermist Dr., Bend, OR 97703, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Ziplyft Forceps Ziplyft

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNR Forceps, Ophthalmic Ophthalmic Class 1 886.4350 2025-04-02
HNN Knife, Ophthalmic Ophthalmic Class 1 886.4350 2023-03-17

Official Correspondent

Knute Buehler

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Osheru
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
K874057 Myocure, Inc. OPHTHALMIC TIP & BLADE SCALPELS 1987-12-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0026-04 Surgical Specialties Corp 1
Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024 Alcon Research LLC Aspex Facility 1
20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024 Alcon Research LLC Aspex Facility 1
ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1925-2024 Alcon Research LLC Aspex Facility 1
ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3026790897. Last updated year: 2026. Please use registration number 3026790897 when referencing this establishment in official correspondence.
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