OKAPI MEDICAL DBA RESIVANT MEDICAL

FDA Device Registration & Listing · Akron, OH, US · Registration 3031294900

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
3031294900
FEI Number
3031294900
Entity Name
OKAPI MEDICAL DBA RESIVANT MEDICAL
City/State/Country
Akron, OH, US
Establishment Address
526 S Main St # 124m, Akron, OH 44311, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Okapi Medical dba Resivant Medical (Owner Number: 10092381)
Owner / Operator Contact Address
526 S. Main St., 124M, Akron, OH 44311, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K234114
PMA Number
N/A

All Registered Proprietary Names

CUTIVA(TM) PLUS Skin Closure System (RM-1739)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MPN Tissue Adhesive For The Topical Approximation Of Skin General, Plastic Surgery Class 2 878.4010 2024-12-30
OMD Cutaneous Tissue Adhesive With Mesh General, Plastic Surgery Class 2 878.4011 2024-12-30

Official Correspondent

Tom Stephens

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Okapi Medical dba Resivant Medical
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 3031294900. Last updated year: 2026. Please use registration number 3031294900 when referencing this establishment in official correspondence.
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