Atlas FDA

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

Symbiosis Corp. · Predicate Candidate Screening

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

117 daysmedian FDA review time
314 days90th percentile
34clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K955119SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESSymbiosis Corp.1996-01-18700
K953453SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODESSymbiosis Corp.1996-01-171820
K953242SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODESSymbiosis Corp.1995-10-06870
K952432SYMBIOSIS BIPOLAR FORCEPSSymbiosis Corp.1995-07-05420
K951387SYMBIOSIS BIPOLAR SCISSORSSymbiosis Corp.1995-04-10140
K950286SYMBIOSIS BIPOLAR SCISSORSSymbiosis Corp.1995-02-03100
K946238SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPSSymbiosis Corp.1995-01-20290
K930773SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPSSymbiosis Corp.1994-07-285270
K941426SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBESymbiosis Corp.1994-06-22900
K932266SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HANSymbiosis Corp.1994-03-153290
K931957SYMBIOSIS DISPOSABLE UROLOGICAL BIOPSY FORCEPSSymbiosis Corp.1994-02-283140
K924016SYMBIOSIS REUSABLE ARTHROSCOPIC SURGICAL INST.Symbiosis Corp.1993-12-064820
K932265SYMBIOSIS DISPOS PULMON BIOPSY FORCEPS W/REUS HANDSymbiosis Corp.1993-08-091110
K931793SYMBIOSIS ENT SURGICAL INSTRUMENTSSymbiosis Corp.1993-07-221010
K930160ILLINOIS STERNAL/ILIAC ASPIRATION NEEDLESymbiosis Corp.1993-07-061740
K930158BONE MARROW BIOPSY PROCEDURE TRAYSymbiosis Corp.1993-07-021700
K926109FLUID DRAINAGE TRAYSymbiosis Corp.1993-06-071860
K925707INSTRUMENT, MANUAL, GENERAL SURGICALSymbiosis Corp.1993-05-261950
K924501GILLAM-TUKEL BONE MARROW BIOPSY NEEDLESymbiosis Corp.1993-04-202280
K924017SYMBIOSIS DISPOSABLE ARTHROSCOPIC SURGICAL INST.Symbiosis Corp.1993-03-162170
K925416SYMBIOSIS BONE MARROW BIOPSY NEEDLESymbiosis Corp.1993-02-231190
K925410SYMBIOSIS HEMOSTATIC WANDSymbiosis Corp.1993-02-231200
K924702TURKEL ABDOMINAL PARACENTESIS SYSTEMSymbiosis Corp.1993-01-121170
K923563SYMBIOSIS SUCTION-IRRIGATORSymbiosis Corp.1992-11-251310
K920762BIOSPSY FORCEPSSymbiosis Corp.1992-08-261890
K922571INSTRUMENT, MANUAL, GENERAL SURGICALSymbiosis Corp.1992-08-11710
K923028TURKEL PNEUMOTHORAX KITSymbiosis Corp.1992-08-04420
K921461TURKEL THORACENTESIS NEEDLESymbiosis Corp.1992-07-301250
K922614TURKEL THORACENTESIS SYSTEMSymbiosis Corp.1992-07-30580
K910831ENDOPATH SURGICAL INSTRUMENTSSymbiosis Corp.1991-05-31930
K910964HOT BIOPSY FORCEPSSymbiosis Corp.1991-05-02570
K910855ENDOPATH VERESS NEEDLESymbiosis Corp.1991-04-18490
K895415BIOPSY FORCEPSSymbiosis Corp.1989-10-31560
K894419GASTRO ENTEROLOGICAL BIOPTOMESymbiosis Corp.1989-09-08530

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