Atlas FDA

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

National Patent Development Corp. — Predicate Candidate Screening

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

34 daysmedian FDA review time
86 days90th percentile
34clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K843974VARIABLE TEMPERATURE CAUTERY DEVICENational Patent Development Corp.1985-02-261380
K832699HYDRON WOUND DRESSING FAST SEAT KITNational Patent Development Corp.1984-04-272610
K822793PIO ROOT CANAL INDICATORNational Patent Development Corp.1982-10-22360
K820028ZEON COMPOSITE RESIN LIGHT CURE SYSNational Patent Development Corp.1982-03-11650
K820006ZEON COMPOSITE RESIN SYSTEMNational Patent Development Corp.1982-01-22180
K811446HYDRON WOUND DRESSING KITNational Patent Development Corp.1981-06-12210
K801484ROOT CANAL FILLING APPLICATOR NEEDLESNational Patent Development Corp.1980-07-21660
K801483MARK IV SYRINGENational Patent Development Corp.1980-07-21660
K801482HYDRON ROOT CANAL FILLING MATERIALNational Patent Development Corp.1980-07-21660
K792136HYPO-ALLERGENIC PLASTIC TAPENational Patent Development Corp.1980-01-16860
K792227MULTI-AD FLUID DISPENSING SYSTEMNational Patent Development Corp.1979-12-20450
K791865HYDRON BURN DRESSING FIELD KITNational Patent Development Corp.1979-11-16560
K792102HYPO-ALLERGENIC CLOTH ADHESIVE TAPENational Patent Development Corp.1979-11-16280
K792103HYPO-ALLERGENIC PAPER ADHESIVE TAPENational Patent Development Corp.1979-11-16280
K792069TRACHEOSTOMY CARE KITNational Patent Development Corp.1979-10-30150
K792021LARGE VOLUME 5 MICRON CONICAL FILTERNational Patent Development Corp.1979-10-26170
K790574EPIC D215National Patent Development Corp.1979-04-30380
K790575TUBE, ARMORED TRACHEALNational Patent Development Corp.1979-04-13210
K790062IV ADMINISTRATION SET WITH BACKCHECKNational Patent Development Corp.1979-04-109061
K790472BURRON VENTED NEEDLENational Patent Development Corp.1979-03-26210
K790060NEEDLE II, BURRON FILTERNational Patent Development Corp.1979-03-21700
K790142NEEDLE, WITH FILTERNational Patent Development Corp.1979-02-26380
K790061NEEDLE, BURRON FILTERNational Patent Development Corp.1979-02-16370
K781744IV SET WITH GRADUATED CHAMBERNational Patent Development Corp.1978-12-07487
K781216INFUSION CONTROLLER, PARENTERALNational Patent Development Corp.1978-08-10240
K781154SYRINGE, INSULIN, HYPOTIPNational Patent Development Corp.1978-08-10310
K780549NON-STICK PADSNational Patent Development Corp.1978-04-19140
K780550STERILE AIR SYRINGENational Patent Development Corp.1978-04-19140
K780551I.V. ADMINISTRATION SET WITH MINI-SPIKENational Patent Development Corp.1978-04-19142
K780106PARENTERAL INFUSION CONTROLLER, ELEC.National Patent Development Corp.1978-02-21320
K771921HYDRON ROOT CANAL FILLING SYSTEMNational Patent Development Corp.1977-11-15340
K770967SYRINGE, ENDODONTIC, W/PERFORATED NEEDLENational Patent Development Corp.1977-06-20200
K770642SYRINGE, ENDODONTIC W/NOTCHED TIP NEEDLENational Patent Development Corp.1977-04-15110
K770124PRE-ROLLED IMPERVIOUS STOCKINETTENational Patent Development Corp.1977-01-2650

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