Atlas FDA

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

Dexide, Inc. — Predicate Candidate Screening

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

42 daysmedian FDA review time
126 days90th percentile
38clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K991814MULTACHOICE INSTRUMENTSDexide, Inc.1999-06-23270
K990379MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIESDexide, Inc.1999-03-04240
K981940MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIESDexide, Inc.1998-09-251150
K981941MULTAPORT CANNULA REDUCER AND ACCESSORIESDexide, Inc.1998-07-29570
K953611DEXIDE ENDO-LUBE KITDexide, Inc.1995-09-15440
K944509DEXIDE INSUFFLATION TUBING WITH FILTERDexide, Inc.1995-02-071450
K924117DEXIDE LAPAROSCOPIC KITSDexide, Inc.1993-03-232210
K923845DEXIDE LAPAROSCOPIC ACCESSORIESDexide, Inc.1992-11-251170
K921709ENDOBAG, MODIFICATIONDexide, Inc.1992-07-141260
K913762MONOSCOPY(TM) BRAND, ENDOBAGDexide, Inc.1991-10-28670
K912637LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLEDexide, Inc.1991-10-041120
K912862MONOSCOPY(TM) BRANK, HOOK DISSECTORDexide, Inc.1991-08-12460
K912750MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTRDexide, Inc.1991-08-02420
K913104MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKEDexide, Inc.1991-07-31190
K912980MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIEDDexide, Inc.1991-07-26320
K912343DISTENDABLE PALPATION PROBEDexide, Inc.1991-06-18210
K905549THE DARTDexide, Inc.1991-02-19700
K902563MONOSCOPY(TM) BRAND, TROCAR REDUCER SETDexide, Inc.1990-09-04850
K896205MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVEDexide, Inc.1990-03-221470
K893527LAPAROSCOPIC SUCTION PROBEDexide, Inc.1989-07-14670
K892001DEX-CELL HYSTEROSCOPY FLUID DELIVERY DEVICEDexide, Inc.1989-06-16800
K854072JOHNS-ALLGOOD IRRIVAC DRIVE-IRRIGATOR/ASPIRATOR-Dexide, Inc.1985-11-15420
K810655DISPOSABLE SCRUB BRUSHDexide, Inc.1981-05-05630
K792270DEXIDE DISPOSABLE PREP STICK W/IODOPHORDexide, Inc.1980-02-08870
K792272DEXIDE DIS. SUR. SCRUB SPONGE W/PARACHLODexide, Inc.1979-12-27440
K792273DEXIDE DIS. PREP SPONGE W/IDEX PATIENT PDexide, Inc.1979-12-10270
K792271DEXIDE DISPOSABLE SURGICAL SCRUB SPONGEDexide, Inc.1979-12-10270
K791949DEXIDE DISPOSABLE SURGICAL SCRUB BRUSHDexide, Inc.1979-10-17160
K791951DEXIDE DISPOSABLE SURGICAL SCRUB SPONGEDexide, Inc.1979-10-17160
K791952DEXIDE DISPOSABLE SURGICAL SCRUB BRUSHDexide, Inc.1979-10-17160
K791950DEXIDE DISPOSABLE SURGICAL SCRUB SPONGEDexide, Inc.1979-10-17160
K791167DEXIDE DISPOSABLE PREP PADDexide, Inc.1979-08-03390
K791168DEXIDE DISPOSABLE PREP STICKDexide, Inc.1979-07-30350
K791169DEXIDE DISPOSABLE SWAB STICKDexide, Inc.1979-07-30350
K791166DEXIDE DISPOSABLE PREP SPONGEDexide, Inc.1979-07-10150
K782173SURGERY BRUSHDexide, Inc.1979-01-10120
K782172BRUSH/SPONGE, DISPOSABLEDexide, Inc.1979-01-10120
K781791BOARD, DISPOSABLE CONTROL COUNTDexide, Inc.1978-11-08190

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