Atlas FDA

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

Worldwide Medical Technologies, LLC — Predicate Candidate Screening

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

84 daysmedian FDA review time
287 days90th percentile
15clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K062214BRACHYSCIENCES STRANDPORTWorldwide Medical Technologies, LLC2007-03-012120
K023179READI-STRAND, MODEL PSSTRANDWorldwide Medical Technologies, LLC2003-07-022810
K022705READI-STRAND, MODEL PSSTRANDWorldwide Medical Technologies, LLC2003-06-092990
K022389READI-LOAD SYSTEM, MODEL PSS 1820RLWorldwide Medical Technologies, LLC2003-05-062870
K020641SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 001Worldwide Medical Technologies, LLC2002-10-292440
K020337READI-STRAND; MODEL PSSTRANDWorldwide Medical Technologies, LLC2002-07-291780
K020867BONE MARROW ASPIRATION NEEDLE, MODEL BMB1110J, BONE MARROW HWorldwide Medical Technologies, LLC2002-05-20630
K991344WORLDWIDE MEDICAL TECHNOLOGIES SEEDING SPACERSWorldwide Medical Technologies, LLC1999-11-052000
K981889WORLDWIDE MEDICAL TECHNOLOGIES INTRODUCER NEEDLEWorldwide Medical Technologies, LLC1998-07-31630
K982097WORLDWIDE MEDICAL TECHNOLOGIES INTRACERVICAL BLOCK NEEDLE, MWorldwide Medical Technologies, LLC1998-06-25100
K981470WORLDWIDE MEDICAL TECHNOLOGIES NEEDLE GUIDEWorldwide Medical Technologies, LLC1998-06-19570
K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE Worldwide Medical Technologies, LLC1998-01-30150
K974794WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY NEEDLEWorldwide Medical Technologies, LLC1998-01-23320
K974118WORLDWIDE MEDICAL TECHNOLOGIES SEED IMPLANT NEEDLE SETWorldwide Medical Technologies, LLC1998-01-23840
K980068WORLDWIDE MEDICAL TECHNOLOGIES I TYPE NEEDLEWorldwide Medical Technologies, LLC1998-01-23150

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