510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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Reliant Technologies, Inc.

Angels Camp, CA, US

Reliant Technologies, Inc. appears in FDA device records in Angels Camp, CA. FDA records list 19 510(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
19
PMA records
0
Recall records
0
Registered establishments
0

510(k) clearance history

FDA records hold 19 510(k) clearances for Reliant Technologies, Inc. between 1994 and 2008. The busiest year on record is 2007, with 6. The most recent is 2008, with 1.

Clearances by year, as a table
510(k) clearance decisions for Reliant Technologies, Inc., by decision year
YearClearances
19942
19951
19961
19971
20032
20041
20052
20062
20076
20081
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K080915FRAXEL RE:PAIR (FRAXEL III SR) LASER SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K071051FRAXEL III SR LASER SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K071621RELIANT TECHNOLOGIES C300 CHILLER SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K070284FRALEX SR 1500 LASER SYSTEM (FRALEX II SR LASER SYSTEM)GEXSubstantially Equivalent
K063808FRAXEL IV SR LASER SYSTEMGEXSubstantially Equivalent
K063038FRAXEL III SR LASER SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K062303FRAXEL II SR LASER SYSTEMGEXSubstantially Equivalent
K060310FRAXEL II SR LASER SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K053047FRAXEL SR LASER SYSTEMGEXSubstantially Equivalent
K050841FRAXEL SR LASER SYSTEMGEXSubstantially Equivalent
K042319RELIANT LASER II SYSTEM AND ACCESSORIESGEXSubstantially Equivalent
K040617RELIANT LASER SYSTEM IIGEXSubstantially Equivalent
K031795RELIANT LASER SYSTEMGEXSubstantially Equivalent
K023050RELIANT BTL 5000 PULS ELECTRICAL STIMULATION SYSTEM, RELIANT BTL 5000 SONO ULTRASOUND SYSTEM, RELIANT BTL 5000 COMBIIMGSubstantially Equivalent
K971821UNICA 315 M CO2 SURGICAL LASER SYSTEMGEXSubstantially Equivalent
K953670ACCUSCAN MODEL C CO2 LASER SCANNERGEXSubstantially Equivalent
K944437DISPOSABLE LASER SWEEP TIPGEXSubstantially Equivalent
K942935ACUTOME 100 COLOR-CORRECTED CO2 LASER HANDPIECEGEXSubstantially Equivalent
K943045UNIMAX MODEL 2500 MULTIWAVELENGTH COLOR CORRECTEDGEXSubstantially 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