ARMIS BIOPHARMA, INC.

FDA Device Registration & Listing · Fort Collins, CO, US · Registration 3020745223

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
3020745223
FEI Number
3020745223
Entity Name
ARMIS BIOPHARMA, INC.
City/State/Country
Fort Collins, CO, US
Establishment Address
2401 Research Blvd Ste 205, Fort Collins, CO 80526, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Armis Biopharma, Inc. (Owner Number: 10083045)
Owner / Operator Contact Address
2401 Research Blvd, Suite 205, Fort Collins, CO 80526, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K220759
PMA Number
N/A

All Registered Proprietary Names

VeriFixx (TM) Small Bone Implant Armis VeriCyn Wound Wash

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2021-10-21
FQH Lavage, Jet General Hospital Class 2 880.5475 2025-11-19
FRO Dressing, Wound, Drug Unknown Class U N/A 2025-11-19

Official Correspondent

Steve Coder

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Armis Biopharma, Inc.
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
K895079 Buckman Co., Inc. ACE BEADED K-WIRES ACE OLIVE WIRES 1989-09-13
K922193 Osteo AG OSTEO KIRSCHNER WIRE 1992-07-23
K850026 Kirkstil Corp., Inc. ORTHOPEDIC IMPLANT NAILS & PINS 1985-05-20
K963367 Rms Div. RMS K-WIRE 1996-10-30
K213616 Becton, Dickinson and Company BD Surgiphor Antimicrobial Irrigation System 2022-03-23

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-05 Biomet, Inc. 2
Lactosorb pin, 2.0 x 20 mm, sterile; ref. 948205.
Z-0003-06 B. Braun Medical, Inc. U
D-Stat Dry Hemostatic Bandage. The product is an adhesive bandage.
Z-0038-2025 3M Company Health Care Business 3m Center U
3M Tegaderm CHG, Chlorhexidine Gluconate I.V. Securement Dressing, REF 1658R

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3015231789 Arthrex Manufacturing Inc. Pendleton, SC, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020745223. Last updated year: 2026. Please use registration number 3020745223 when referencing this establishment in official correspondence.
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