INTEGRATED ORBITAL IMPLANTS, INC.

FDA Device Registration & Listing · SAN DIEGO, CA, US · Registration 2027377

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
2027377
FEI Number
3009688114
Entity Name
INTEGRATED ORBITAL IMPLANTS, INC.
City/State/Country
SAN DIEGO, CA, US
Establishment Address
11230 Sorrento Valley Rd Ste 135, SAN DIEGO, CA 92121, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
INTEGRATED ORBITAL IMPLANTS INC (Owner Number: 2027377)
Owner / Operator Contact Address
11230 Sorrento Valley Rd Ste 135, --, San Diego, CA 92121, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Needle, ophthalmic suturing IMPLANT, EYE SPHERE THREADED SLEEVE DRIVER THREADED SLEEVE WRENCH

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HNM Needle, Ophthalmic Suturing Ophthalmic Class 1 886.4350 2006-12-11
HPZ Implant, Eye Sphere Ophthalmic Class 2 886.3320 2007-11-13
LRZ Screwdriver, Surgical General, Plastic Surgery Class 1 878.4800 2024-02-29

Official Correspondent

Vicki Perry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

INTEGRATED ORBITAL IMPLANTS INC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0012-2007 Integrated Orbital Implants Inc 2
Bio-Eye Hydroxyapatite (HA) Orbital Implant and Conformer, Model Number: 100020S
Z-0040-2018 Genesys Orthopedics Systems, LLC 1250 S Capital of Texas Hwy Ste 600 Bldg # 3 West Lake Hills TX 78746-6446 1
Genesys spine, Binary Screwdriver, GCP221, component of the Binary Anterior Cervical Plating System The Genesys Spine Binary Anterior Cervical Plate System is intended for anterior screw fixation to the cervical spine. It is to be used in skeletally mature patients as an adjunct to fusion of the cervical spine (C2 to C7). The system is indicated for use in the temporary stabilization of the anterior spine during the development of cervical spinal fusion in patients with degenerative disc disease (as defined by neck pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies), spondylolisthesis, trauma (i.e. fractures or dislocations), tumors, deformity (defined as kyphosis, lordosis, or scoliosis),pseudoarthrosis, failed previous fusion, and/or spinal stenosis.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2027377. Last updated year: 2026. Please use registration number 2027377 when referencing this establishment in official correspondence.
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