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Mentor O & O, Inc.

Mchenry, IL, US

Mentor O & O, Inc. appears in FDA device records in Mchenry, IL. FDA records list 18 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.

FDA records held for this company

510(k) clearances
18
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 18 510(k) clearances for Mentor O & O, Inc. between 1982 and 1996. The busiest year on record is 1985, with 3. The most recent is 1996, with 1.

Clearances by year, as a table
510(k) clearance decisions for Mentor O & O, Inc., by decision year
YearClearances
19821
19842
19853
19882
19893
19901
19912
19922
19941
19961
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K955245MENTOR MERIDIAN PHACOEMULSIFICATION SYSTEMHQCSubstantially Equivalent
K934320MENTOR WET-FIELD HEMOSTATIC ERASER BIPOLAR INSTRUMENT, 20 GAUGE WITH EXTRUSION ASPIRATIONHQRSubstantially Equivalent
K912904MENTOR ODYSSEY PHACOEMULSIFICATION SYSTEMHQCSubstantially Equivalent
K915340MENTOR HORIZON LOW VISION MAGNIFIERHJGSubstantially Equivalent
K910637MENTOR(R) SUR-E-TROL(R)FRNSubstantially Equivalent
K911160MENTOR(R) WET-FIELD(R) II AC COAGULATOR, 22-1305GEISubstantially Equivalent
K903878MENTOR(R) DURASTAT(TM) AUTOCLAV BIPOLAR HEMOSTATHQQSubstantially Equivalent
K895010MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPEHLISubstantially Equivalent
K890622SURG-E-TROL SYSTEM I AND SYSTEM IIHQESubstantially Equivalent
K890595MENTOR ANTERIOR SEGMENT VITRECTORHKPSubstantially Equivalent
K881001MENTOR WET-FIELD*II COAGULATORHQQSubstantially Equivalent
K875112MENTOR B-VAT(TM) II VIDEO TESTERHOXSubstantially Equivalent
K853736MENTOR BRIGHTNESS ACUITY TESTERHOXSubstantially Equivalent
K853382MAID MENTOR ASPIRATION/IRRIGATION DEVROHQESubstantially Equivalent
K850270CORNEAL LIGHT SHIELDHRMSubstantially Equivalent
K844129SHURE GRIP TYING FORCEPSHNRSubstantially Equivalent
K843304BINOCULAR INDIRECT OPHTHALMOSCOPEHLISubstantially Equivalent
K821932MENTOR POTENTIAL ACUITY METERHOXSubstantially Equivalent

Registered establishments

No FDA establishment registrations recorded against this company.

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