BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.

FDA Device Registration & Listing · KIRYAT MALACHI Southern, IL · Registration 3000164186

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
3000164186
FEI Number
3000164186
Entity Name
BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.
City/State/Country
KIRYAT MALACHI Southern, IL
Establishment Address
BE'ER TUVIA INDUSTRIAL ZONE, P.O. BOX 571, KIRYAT MALACHI Southern 83104, IL
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
FERRING PHARMACEUTICALS INC. (Owner Number: 2244564)
Owner / Operator Contact Address
100 Interpace Parkway, Parsippany, NJ 07054, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BIOLON EUFLEXXA

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LZP Aid, Surgical, Viscoelastic Ophthalmic Class 3 886.4275 2004-08-26
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2004-08-26

Official Correspondent

No official correspondent registered.

US Agent Details

Kevin Wyckoff Business: Ferring Pharmaceuticals, Inc. Email: kevin.wyckoff@ferring.com Phone: (973) 2064987

Related Public Records

Same Entity

FERRING PHARMACEUTICALS INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
2244564 FERRING PHARMACEUTICALS INC. PARSIPPANY, NJ, US

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 3000164186. Last updated year: 2026. Please use registration number 3000164186 when referencing this establishment in official correspondence.
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