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Alcon Grieshaber AG

Schaffhausen, CH

ALCON GRIESHABER AG appears in FDA device records in Schaffhausen, CH. FDA records list no 510(k) clearances, no PMA records and 2 registered establishments. As of , FDA records show one recall for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
0
PMA records
0
Recall records
1
Registered establishments
2

510(k) clearance history

No 510(k) clearance records for this company in the ingested FDA data.

No 510(k) clearance records in the ingested FDA data.

Registered establishments

FDA registered establishments for Alcon Grieshaber AG, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30033988733003398873ALCON GRIESHABER AGWINKELRIEDSTRASSE 52, SCHAFFHAUSEN 8203 CH2026and 3 more, listed in full below
30334859553033485955ALCON GRIESHABER AGVictor von Bruns-Strasse 21, Neuhausen Schaffhausen 8212 CH2026and 2 more, listed in full below

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

Device recall records naming this company, most recent first
RecallProductReasonClassificationInitiatedStatus
Z-1506-2013The Constellation Vision System Pneumatic Handpiece. Indicated for both anterior and posterior segment opthalmic surgery.Alcon is conducting a Medical Device Removal for the Constellation Pneumatic Handpiece, DSP, product number 725.01. This action is being taken because the forceps or scissors tips (sold separately) may dislodge from the hand piece, if not attached by the user according to the Directions for Use.Class IITerminated

Verification record

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Data as of , FDA export datePage updated Source: openFDA, public domain