FDA.reportPublic FDA data

Surgical Direct

Primary DI
B382SD9176201020
Brand
Surgical Direct
Company
Surgical Direct, Inc.
Model
SD917620102
Catalog number
SD917620102
Device description
2 7/16” x 7/8” Hill-Ferguson Rectal Retractor
Published
2026-07-13
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MDMInstrument, Manual, Surgical, General UseGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B382SD9176201020PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Hand-held surgical retractor, reusableA hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; it is not dedicated to ophthalmic surgery or small nerve/vessel retraction, but may otherwise be clinically dedicated. It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1 (800) 519-3293info@surgicaldirect.com

Regulatory Flags#

DUNS number
124367223
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B382SD9141791400Surgical DirectSD914179140SD9141791402026-07-13
B382SD9142211000Surgical DirectSD914221100SD9142211002026-07-13
B382SD914264010Surgical DirectSD91426401SD914264012026-07-13
B382SD914341100Surgical DirectSD91434110SD914341102026-07-13
B382SD9143681000Surgical DirectSD914368100SD9143681002026-07-13
B382SD91705515T0Surgical DirectSD91705515TSD91705515T2026-07-13
B382SD91705525T0Surgical DirectSD91705525TSD91705525T2026-07-13
B382SD918006150Surgical DirectSD91800615SD918006152026-07-13
B382SD918006200Surgical DirectSD91800620SD918006202026-07-13
B382SD918174150Surgical DirectSD91817415SD918174152026-07-13
B382SD9183701030Surgical DirectSD918370103SD9183701032026-07-13
B382SD9183761030Surgical DirectSD918376103SD9183761032026-07-13
B382SD9184571000Surgical DirectSD918457100SD9184571002026-07-13
B382SD9184932000Surgical DirectSD918493200SD9184932002026-07-13
B382SD9153301000Surgical DirectSD915330100SD9153301002022-12-05
B382SD883110450Surgical DirectSD88311045SD883110452026-07-10
B382SD88324450Surgical DirectSD8832445SD88324452026-07-10
B382SD9032161000Surgical DirectSD903216100SD9032161002026-07-10
B382SD90390213SC0Surgical DirectSD90390213SCSD90390213SC2026-07-10
B382SD9044561000Surgical DirectSD904456100SD9044561002026-07-10

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Primary DI, Brand, Company table
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00850088713046PRINCETONPrinceton Medical Group, Inc.MDM2026-07-10
00850088713053PRINCETONPrinceton Medical Group, Inc.MDM2026-07-10
03661219436522LANDANGERLANDANGERMDM2026-07-08
03661219436584LANDANGERLANDANGERMDM2026-07-08
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