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Medical Device Inspection Company

Great Neck, NY, US

MEDICAL DEVICE INSPECTION COMPANY appears in FDA device records in Great Neck, NY. FDA records list 30 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.

FDA records held for this company

510(k) clearances
30
PMA records
0
Recall records
0
Registered establishments
1

510(k) clearance history

FDA records hold 30 510(k) clearances for Medical Device Inspection Company between 1990 and 1995. The busiest year on record is 1991, with 13. The most recent is 1995, with 1.

Clearances by year, as a table
510(k) clearance decisions for Medical Device Inspection Company, by decision year
YearClearances
19905
199113
19925
19935
19941
19951
510(k) clearances on record, most recent first
K numberDeviceProduct codeDecisionDecision date
K945826J & J I-330 SERIES PHYSIOLOGICAL MONITORING & BIOFEEDBACK INSTUMENT AND USE SOFTWARE APPLICATIONSHCCSubstantially Equivalent
K932072JARIT SURGICAL INSTRUMENTSHETSubstantially Equivalent
K931594THERA-TURN CM-1000 MATTRESS OVERLAY SYSTEMIOQSubstantially Equivalent
K933581POWERMATIC TREATMENT TABLEINQSubstantially Equivalent
K933580POWER WORK TABLEINQSubstantially Equivalent
K933578POWERMATIC MAT PLATFORMINQSubstantially Equivalent
K933577POWERMATIC EXAMINATION TABLEINQSubstantially Equivalent
K922045SHOWER CHAIRSINMSubstantially Equivalent
K912075C-SECTION TRAYKNAUnknown
K914174STERILE DISPOSABLE WET SKIN SCRUB TRAYLROUnknown
K920403XENON ARC ENDOSCOPE LIGHT SOURCEGCJSubstantially Equivalent
K912054LABOR DELIVERY TRAYHFWUnknown
K912158CENTRAL VENOUS CATHETER DRESSING CHANGE TRAYFOZUnknown
K912116PRESSURE SORE MANAGEMENT KITMCYSubstantially Equivalent
K913643MUCOUS SPECIMEN TRAPBYZSubstantially Equivalent
K912161I.V. STARR KITLKBSubstantially Equivalent
K913223STERILE DISPOSABLE URINE COLLECTOR & ACCESSORIESKNXSubstantially Equivalent
K912159MAJOR SET-UP TRAYGCJSubstantially Equivalent
K912106ARTHROSCOPY TRAYFSMSubstantially Equivalent
K912105EYE TRAYLRPSubstantially Equivalent
K912053OPEN HEART TRAYFSMSubstantially Equivalent
K912052HEART CATH TRAYFSMSubstantially Equivalent
K912117LACERATION TRAYMCYSubstantially Equivalent
K912104MAJOR BASIN TRAYFSMSubstantially Equivalent
K911081LATEX PATIENT EXAMINATION GLOVESLYYSubstantially Equivalent
K904034TEMPORARY DENTAL CEMENTEMASubstantially Equivalent
K905550PATIENT EXAMINATION GLOVESLYYSubstantially Equivalent
K902893TI-CORE (DENTAL COMPOSITE)EBFSubstantially Equivalent
K902894POST CEMENT (DENTAL COMPOSITE)EMASubstantially Equivalent
K893229SPATULA FOR PAP SMEAR COLLECTIONHHTSubstantially Equivalent

Registered establishments

FDA registered establishments for Medical Device Inspection Company, with the product codes listed at each
RegistrationFEIEstablishmentAddressRegistration expiresProduct codes listed
30100348503010034850MEDICAL DEVICE INSPECTION COMPANY55 Northern Blvd Suite 200, Great Neck, NY 11021 US2026No device listings on this registration

Registration numbers link to the FDA registration and listing record for that establishment.

FDA product codes

Recall records

No recall records for this company in the ingested FDA data.

Verification record

There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.

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Data as of , FDA export datePage updated Source: openFDA, public domain