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Surgistar, Inc.

Vista, CA, US

SURGISTAR, INC. appears in FDA device records in Vista, CA. FDA records list 4 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
4
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 4 510(k) clearances for Surgistar, Inc. between 1992 and 2003. The busiest year on record is 1992, with 1. The most recent is 2003, with 1.

Clearances by year, as a table
510(k) clearance decisions for Surgistar, Inc., by decision year
YearClearances
19921
19941
19991
20031
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K030891SURGISTAR MICROKERATOME BLADE, MODEL NO. 2400-LSKHNOSubstantially Equivalent
K992978RICROKERATOME BLADEHNOSubstantially Equivalent
K941747SURGISTAR TROCARSGCJSubstantially Equivalent
K923689SURGISTAR BLADESGDXSubstantially Equivalent

Registered establishments

FDA registered establishments for Surgistar, Inc., with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
20286613005765014SURGISTAR, INC.2310 la Mirada Dr, VISTA, CA 92081 US2026

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

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

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