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-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K991814 | MULTACHOICE INSTRUMENTS | Dexide, Inc. | 1999-06-23 | 27 | 0 |
| K990379 | MODIFICATION TO MULTAPORT CANNULA, REDUCER AND ACCESSORIES | Dexide, Inc. | 1999-03-04 | 24 | 0 |
| K981940 | MULTAPUMP DISPOSABLE PUMP HEAD AND ACCESSORIES | Dexide, Inc. | 1998-09-25 | 115 | 0 |
| K981941 | MULTAPORT CANNULA REDUCER AND ACCESSORIES | Dexide, Inc. | 1998-07-29 | 57 | 0 |
| K953611 | DEXIDE ENDO-LUBE KIT | Dexide, Inc. | 1995-09-15 | 44 | 0 |
| K944509 | DEXIDE INSUFFLATION TUBING WITH FILTER | Dexide, Inc. | 1995-02-07 | 145 | 0 |
| K924117 | DEXIDE LAPAROSCOPIC KITS | Dexide, Inc. | 1993-03-23 | 221 | 0 |
| K923845 | DEXIDE LAPAROSCOPIC ACCESSORIES | Dexide, Inc. | 1992-11-25 | 117 | 0 |
| K921709 | ENDOBAG, MODIFICATION | Dexide, Inc. | 1992-07-14 | 126 | 0 |
| K913762 | MONOSCOPY(TM) BRAND, ENDOBAG | Dexide, Inc. | 1991-10-28 | 67 | 0 |
| K912637 | LAPAROSCOPIC ELECTROSURGICAL CANNULA W/RETRACTABLE | Dexide, Inc. | 1991-10-04 | 112 | 0 |
| K912862 | MONOSCOPY(TM) BRANK, HOOK DISSECTOR | Dexide, Inc. | 1991-08-12 | 46 | 0 |
| K912750 | MONOSCOPY(TM) BRAND, DUAL SUCTION/IRRIGATION CONTR | Dexide, Inc. | 1991-08-02 | 42 | 0 |
| K913104 | MONOSCOPY(TM) BRAND, ELECTROSURGICAL RAKE | Dexide, Inc. | 1991-07-31 | 19 | 0 |
| K912980 | MONOSCOPY BRAND 5MM LOCK TROCAR SLEEVE, MODIFIED | Dexide, Inc. | 1991-07-26 | 32 | 0 |
| K912343 | DISTENDABLE PALPATION PROBE | Dexide, Inc. | 1991-06-18 | 21 | 0 |
| K905549 | THE DART | Dexide, Inc. | 1991-02-19 | 70 | 0 |
| K902563 | MONOSCOPY(TM) BRAND, TROCAR REDUCER SET | Dexide, Inc. | 1990-09-04 | 85 | 0 |
| K896205 | MONOSCOPY BRAND, 5 MM LOCKING TROCAR SLEEVE | Dexide, Inc. | 1990-03-22 | 147 | 0 |
| K893527 | LAPAROSCOPIC SUCTION PROBE | Dexide, Inc. | 1989-07-14 | 67 | 0 |
| K892001 | DEX-CELL HYSTEROSCOPY FLUID DELIVERY DEVICE | Dexide, Inc. | 1989-06-16 | 80 | 0 |
| K854072 | JOHNS-ALLGOOD IRRIVAC DRIVE-IRRIGATOR/ASPIRATOR- | Dexide, Inc. | 1985-11-15 | 42 | 0 |
| K810655 | DISPOSABLE SCRUB BRUSH | Dexide, Inc. | 1981-05-05 | 63 | 0 |
| K792270 | DEXIDE DISPOSABLE PREP STICK W/IODOPHOR | Dexide, Inc. | 1980-02-08 | 87 | 0 |
| K792272 | DEXIDE DIS. SUR. SCRUB SPONGE W/PARACHLO | Dexide, Inc. | 1979-12-27 | 44 | 0 |
| K792273 | DEXIDE DIS. PREP SPONGE W/IDEX PATIENT P | Dexide, Inc. | 1979-12-10 | 27 | 0 |
| K792271 | DEXIDE DISPOSABLE SURGICAL SCRUB SPONGE | Dexide, Inc. | 1979-12-10 | 27 | 0 |
| K791949 | DEXIDE DISPOSABLE SURGICAL SCRUB BRUSH | Dexide, Inc. | 1979-10-17 | 16 | 0 |
| K791951 | DEXIDE DISPOSABLE SURGICAL SCRUB SPONGE | Dexide, Inc. | 1979-10-17 | 16 | 0 |
| K791952 | DEXIDE DISPOSABLE SURGICAL SCRUB BRUSH | Dexide, Inc. | 1979-10-17 | 16 | 0 |
| K791950 | DEXIDE DISPOSABLE SURGICAL SCRUB SPONGE | Dexide, Inc. | 1979-10-17 | 16 | 0 |
| K791167 | DEXIDE DISPOSABLE PREP PAD | Dexide, Inc. | 1979-08-03 | 39 | 0 |
| K791168 | DEXIDE DISPOSABLE PREP STICK | Dexide, Inc. | 1979-07-30 | 35 | 0 |
| K791169 | DEXIDE DISPOSABLE SWAB STICK | Dexide, Inc. | 1979-07-30 | 35 | 0 |
| K791166 | DEXIDE DISPOSABLE PREP SPONGE | Dexide, Inc. | 1979-07-10 | 15 | 0 |
| K782173 | SURGERY BRUSH | Dexide, Inc. | 1979-01-10 | 12 | 0 |
| K782172 | BRUSH/SPONGE, DISPOSABLE | Dexide, Inc. | 1979-01-10 | 12 | 0 |
| K781791 | BOARD, DISPOSABLE CONTROL COUNT | Dexide, Inc. | 1978-11-08 | 19 | 0 |
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