CIMA TECHNOLOGY, INC.

FDA Device Registration & Listing · Pittsburgh, PA, US · Registration 2529709

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
2529709
FEI Number
1000121259
Entity Name
CIMA TECHNOLOGY, INC.
City/State/Country
Pittsburgh, PA, US
Establishment Address
480 Davidson Rd, Pittsburgh, PA 15239, US
Establishment Type(s)
Manufacture Device in the United States for Export Only
Owner / Operator
CIMA TECHNOLOGY, INC. (Owner Number: 9005400)
Owner / Operator Contact Address
480 Davidson Road, --, Pittsburgh, PA 15239, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MRJ Ring, Endocapsular Unknown Class 3 N/A 2017-12-29
MSS Folders And Injectors, Intraocular Lens (Iol) Ophthalmic Class 1 886.4300 2018-01-10
LZP Aid, Surgical, Viscoelastic Ophthalmic Class 3 886.4275 2017-12-29
HQL Intraocular Lens Ophthalmic Class 3 886.3600 2008-05-09

Official Correspondent

Carina Navarro

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CIMA TECHNOLOGY, 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-0530-2015 Abbott Medical Optics Inc (AMO) 3
Abbott Healon EndoCoat Ophthalmic Viscosurgical Device 3% sodium hyaluronate 0.85 mL 30 mg/mL Sterile A Solution Sterile EO Packaging and Cannula Product of USA Abbott Healon Duet Dual Pack 0.55 ml OVD 0.85 ml Healon EndoCoat OVD Contents: -one sterile syringe of Healon Ophthalmic Viscosurgical Device (OVD) 0.55 ml (10 mg/ml Sodium Hyaluronate) -one sterile syringe of Healon EndoCoat Ophthalmic Viscosurgical Device (OVD) 0.85 ml (30 mg/ml Sodium Hyaluronate) Part Number: US: VT585U and 57502000 (packaged in Healon Duet 10290080) OUS: VT585 and 57550500 (packaged in Healon duet 10220010, 10220011 and 10220012)
Z-2062-2017 Abbott Medical Optics Inc. (AMO) 3
Healon, Part No. 10290953, 10295210, 10200011, 10200012, 10201012, 10203012, 10213012, 10223012, 10290701, 10294751, 10295701
Z-2063-2017 Abbott Medical Optics Inc. (AMO) 3
Healon GV, Part No. 10294701, 10294801, 10200014, 10201014, 10202014, 10203014
Z-2064-2017 Abbott Medical Optics Inc. (AMO) 3
Healon Duet, Part No. 10290080, 10220010, 10220011 and 10220012
Z-2065-2017 Abbott Medical Optics Inc. (AMO) 3
Healon 5 Pro, Part No. 10270015

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2529709. Last updated year: 2026. Please use registration number 2529709 when referencing this establishment in official correspondence.
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