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Breg, Inc.

Vista, CA, US

Breg, Inc. appears in FDA device records in Vista, CA. FDA records list 11 510(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
11
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 11 510(k) clearances for Breg, Inc. between 1995 and 2007. The busiest year on record is 2000, with 3. The most recent is 2007, with 1.

Clearances by year, as a table
510(k) clearance decisions for Breg, Inc., by decision year
YearClearances
19951
19962
19981
20003
20011
20021
20041
20071
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K070402MODIFICATION TO POLAR CARE 500ILOSubstantially Equivalent
K041714E-PAIN CAREFRNSubstantially Equivalent
K020988PAIN CARE 4200MEBSubstantially Equivalent
K013928PAIN CARE 3200MEBSubstantially Equivalent
K003611PAIN CARE MULTI-PORT CATHETER, MODEL 2000LFRNSubstantially Equivalent
K002073PAIN CARE 3000MEBSubstantially Equivalent
K002321PAIN CARE 2000LMEBSubstantially Equivalent
K983454PAIN CARE 2000MEBSubstantially Equivalent
K963596POLAR CARE 300ILOSubstantially Equivalent
K961855POLAR CARE (MODEL 500/50000)ILOSubstantially Equivalent
K950755FLEXMATE K500BXBSubstantially 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