Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Sybron Corp. — Predicate Candidate Screening

37 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

33 daysmedian FDA review time
65 days90th percentile
37clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K862284SEALITESybron Corp.1986-06-2370
K854855PROOF ALGINATE IMPRESSION MATERIALSybron Corp.1986-01-30560
K844092DIAGNOSTIC MICROSOPCE SLIDESSybron Corp.1984-10-2560
K842132TYCOS SELF-CHECK/DIGITAL FEVER THERMOSybron Corp.1984-07-18490
K841910KERR SEALAPEX ROOT CANAL SEALERSybron Corp.1984-07-13650
K841732LIEBEL-FLARSHEIM AFC 1000 X-RAY FILMSybron Corp.1984-06-05400
K840469TYCOS SELF CHECK BPM3 BLOOD PRESS MONISybron Corp.1984-05-211080
K840407KERR RESIN BONDED BRIDGE CEMENTSybron Corp.1984-05-211110
K840607LF MOTORIZED RADIOGRAPHIC FILM VIEWERSybron Corp.1984-03-05210
K833138DIGITAL INJECTOR SYSSybron Corp.1983-11-14610
K823795EVERBOND GLASS IONOMER CEMENTSybron Corp.1983-01-26300
K822869COMMAND BONDING RESIN/GLAZE/OPAQUERSybron Corp.1982-10-13160
K820783CASTLE MICROCOMPUTER STERILIZER CONTROLSybron Corp.1982-04-15230
K820681CASTLE(R) 2510 & 2610 MINOR SURG. LIGHTSybron Corp.1982-04-15350
K820494SYBRON BOVIE CSV HAND CONTR. ELECTROSURGSybron Corp.1982-04-09450
K820182SYBRON/KERR COMMANDSybron Corp.1982-03-02390
K820135TAYLOR & TYCOS ACOUSTIC SPHYGMOMANOMETERSybron Corp.1982-03-01420
K820183SYBRON/KERR MIRROR 3Sybron Corp.1982-02-24330
K820181SYBRON/KERR CONTOURSybron Corp.1982-02-24330
K813201CASTLE #3241 GAS AERATORSybron Corp.1981-12-31480
K812272CASTLE TEC-TEST BIOLOGICAL INDICATORSybron Corp.1981-09-08260
K811728CASTLE & RITTER MINOR SURG. & EXAM LTSybron Corp.1981-07-20320
K811519K-FLEXSybron Corp.1981-06-26290
K810614CASTLE STEAM STERILIZATION INDICATORSybron Corp.1981-06-241070
K810900CASTLE PROCEDURE AND RITTER EXAM. TABLESSybron Corp.1981-04-21180
K802827BOUIE ELECTROSURGICAL TIP CLEANERSybron Corp.1980-12-11310
K801529KERR CORE COMPOSITESybron Corp.1980-08-04330
K801530COREFORM MOLDSSybron Corp.1980-07-28260
K801309RITTER STERILIZERSybron Corp.1980-06-20170
K800276RITTER MODEL H COMPANION STOOLSybron Corp.1980-03-17380
K792648UNILAB CULTURING SETSybron Corp.1980-02-06470
K792060TEMPTRONIC 100 WATER BATHSybron Corp.1979-12-04500
K791699HYDRADJUST II UROLOGICAL TABLESybron Corp.1979-10-22540
K791767BOVIE CSV HAND CONTROL ADAPTERSybron Corp.1979-10-11360
K790187BOVIE HAND CONTROLSybron Corp.1979-02-27290
K772164PANORAMIC X-RAY SYSTEM MODEL ASybron Corp.1977-12-02150
K770812HANDLES, LIGHT, SURGICAL, STEOILESybron Corp.1977-05-23200

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda